job description for medical research associate

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How to Become a Clinical Research Associate

A clinical research associate acts as a liaison between research sponsors and the clinics conducting research. Here’s how you can become one.

Every pill, vaccine, procedure, therapy, or medical device that might be prescribed or used on you to improve your physical or mental health undergoes clinical research trials. During these trials, a drug might get approved for the Food and Drug Administration (FDA) or a medical device approved for consumer or hospital use. 

Clinical research associates (CRA) play a critical role in the health care industry and improving public health . They act as liaisons between those who sponsor research and those who facilitate clinical research. Even prior to the COVID-19 pandemic, rising population density and international travel have increased the spread of new and existing diseases. Clinical research is necessary to gain evidence-based insights on how well a drug or vaccine does.

A career as a clinical research associate can be rewarding for individuals who are excited by the prospect of a dynamic role overseeing many different kinds of clinical trials. Here’s how to get started.

What is a clinical research associate?

Clinical research associates, also called “monitors,” are individuals who act as liaisons between the institutions that sponsor and fund the clinical research trials, and the clinics that conduct the research. They are in charge of making sure the clinical trials run smoothly, monitoring all the procedures, processes, and results, ensuring the researchers are following established guidelines and protocols every step of the way. 

A clinical research associate works on behalf of the sponsor (pharmaceutical company, university, or health organization) or for a contract research organization (CRO). The CRO typically funds the research. Clinical trials are the long, scientific process of ensuring that certain drugs, therapies, and devices are safe and effective for public consumption and use. CRAs guide the trials forward in accordance with regulations for ethics and safety.

Clinical research associates work on a team of research professionals. This is the hierarchy:

Contract research organization (CRO) or sponsor (university, pharmaceutical company)

Principal investigator (PI)

Clinical research associate (CRA)

Clinical research coordinator (CRC)

Clinical research associate job description

As a clinical research associate, these are the typical tasks and responsibilities:

Monitor the clinical research process, including managing supplies and coordination

Oversee data collection and documentation, and inputting data into systems databases

Outline the trial objectives and present the trial protocols to a committee

Coordinate with an ethics committee that protects trial subject confidentiality

Prepare post-trial reports and manage creating the publications

Field-based CRAs travel to different locations to deal with medical professionals in clinics or hospitals. Some CROs hire in-house CRAs to focus only on document review and management, making only occasional site visits.

Where you’ll work

Skills needed.

Clinical research associates need to have certain skills to get hired and be successful in their roles. Whether or not you currently possess these skills, it is possible to learn and acquire them through taking online courses or on the job. Some important skills you’ll need include: 

Administrative skills, including the ability to document important information accurately

IT and computer skills, such as databases and systems management

Written and oral communication skills

Keen attention to detail and organization

Ability to manage and coordinate with several stakeholders

Strong understanding of the clinical research trials and health care space, along with medical terminology

Clinical research associate salary and job outlook

The salary for a clinical research associate can vary depending on your organization and experience level. Clinical research associates can earn a median salary of $95,310 per year, according to the US Bureau of Labor Statistics [ 1 ]. On Glassdoor, the average annual base salary is $69,236 and a total salary of $108,425 [ 2 ].

Clinical research associate was ranked fourth on CNN Money’s Best Jobs in America in 2012, which listed the median pay as $90,800 with a top pay of $129,000 [ 3 ]. Overall, the salary for this role can be high.

How to become a clinical research associate.

A career as a CRA can be fulfilling because you are essentially a part-translator, part-project manager, and part administrator for trials that have the potential to save lives. Here’s how to get started as a clinical research associate.

1. Earn a degree.

To become a CRA, you’ll want to earn a bachelor’s degree in a health-related field. Consider a major in health sciences, nursing, medical technology, or biological sciences. Degrees in the humanities or social sciences, such as sociology or psychology, can also be helpful in providing a strong framework for research insights as a CRA. The degree should provide the foundation you’ll need to pursue clinical research associate and technician roles. 

2. Get certified.

While you do not need a certification to become a clinical research associate, having one can differentiate you from other candidates when it comes to being hired or promoted in this role. You can choose from certifications offered by two different organizations. 

The Association of Clinical Research Professionals (ACRP)

The ACRP offers the Certified Clinical Research Associate credential. To earn this certification, you must have one of the following:

A bachelor’s degree and at least 3,000 hours of experience as a CRA

A current CCRC, CPI or ACRP-CP certification and be able to substitute 1,500 hours of work experience

Completed a clinical research degree program and be able to substitute 1,500 hours of work experience

CCRA applicants must submit proof of their current job description and resume, and pass the CCRA exam. They must also complete 24 hours of continuing education, and be recertified every two years in order to maintain their certification. Through the ACRP, you can also become certified as a research coordinator, principal investigator, and clinical professional.

The Society of Clinical Research Associates (SOCRA)

The SOCRA offers the Certified Clinical Research Professional (CCRP) credential. To earn this certification, you must have one of the following:

At least two years of clinical research experience or 3,500 hours of part-time experience in the past five years

A degree in clinical research and at least one year of full-time experience

A certificate in clinical research, a bachelor’s or associate degree in health science, science, or a related field, and at least one year of full-time work experience

SOCRA applicants must pass the CCRP exam, and be recertified every three years. To become recertified, you’ll need to complete 45 hours of continuing education. 

The main difference between the certifications offered by SOCRA and ACRP is that ACRP only certifies clinical research associates, but SOCRA’s CCRP certification applies to other types of clinical research professionals.

3. Apply for jobs.

When you have the necessary qualifications to become a CRA, you can start applying for jobs. Visit job sites such as Indeed or LinkedIn and type in “clinical research associate” to search for entry or junior-level positions.

Looking for your first job? Read this: How to Get Your First Job: A Guide

Make sure to enhance your resume with any health care-related experiences you may have, including volunteer activities and internships. You’ll want to quantify your accomplishments with statements such as: “I managed clinical trials in seven different states in 2020.”

Prepare for interviews by researching the company and preparing your best answers. Don’t forget to write up a list of questions to ask your interviewer. 

4. Continue learning.

Going on to earn a master’s degree can help you land a managerial position or salary boost as a CRA. Clinical research associates are needed in many different types of organizations, so there are plenty of opportunities to achieve more interesting and dynamic job opportunities when you pursue higher education. 

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Launch your career in the health care industry by honing your skills in medical terminology. You’ll be able to identify parts of words commonly used in medicine, understand health records, and more with the Medical Terminology specialization from Rice University.

Article sources

US Bureau of Labor Statistics. " Occupational Outlook Handbook: Medical Scientists , https://www.bls.gov/ooh/life-physical-and-social-science/medical-scientists.htm." Accessed September 13, 2022.

Glassdoor. " Clinical Research Associate Salaries , https://www.glassdoor.com/Salaries/clinical-research-associate-salary-SRCH_KO0,27.htm." Accessed September 13, 2022.

CNN Money. " Best Jobs in America, 4. Clinical Research Associate , https://money.cnn.com/pf/best-jobs/2012/snapshots/4.html." Accessed September 13, 2022.

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Clinical Research Associate Job Description

Clinical research associates manage clinical trials and studies pertaining to biotechnological and pharmaceutical products, drugs, and procedures. A clinical research associate, also known as a CRA, conducts research to ensure these products are safe to allow on the market.

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Clinical Research Associate Job Description Template

We are looking for an organized, flexible clinical research associate to oversee clinical trials. The clinical research associate will develop and outline trial protocols, establish trial sites, train site staff, and manage Investigational Product (IP) and trial materials. The clinical research associate will manage multiple aspects of the subjects' welfare. You will conduct regular site visits, generate and distribute internal and external newsletters, prepare final reports, and liaise with interested parties regarding all trial aspects. You will play a leading role in generating and overseeing documentation and records.

To be successful in this role, you should be able to recognize logistical problems and initiate appropriate solutions. Ideal candidates will be detail-oriented, have the ability to multitask, and be able to collaborate with various role players.

Clinical Research Associate Responsibilities:

• Creating and writing trial protocols, and presenting these to the steering committee.
• Identifying, evaluating, and establishing trial sites, and closing sites down on completion of the trial.
• Training site staff on therapeutic areas, protocol requirements, proper source documentation, and case report form completion.
• Liaise with the ethics committee regarding the rights, safety, and well-being of trial subjects.
• Ordering, tracking, and managing IP and trial materials.
• Overseeing and documenting IP dispensing inventory, and reconciliation.
• Protecting subjects’ confidentiality, updating their information, and verifying IP have been dispensed and administered according to protocol.
• Conducting regular site visits, coordinating project meetings, and writing visit reports.
• Implementing action plans for sites not meeting expectations.
• Liaising with regulatory authorities.
• Ensuring compliance with SOPs and local regulations, and ICH and GCP guidelines.
• Other tasks and responsibilities as needed.

Clinical Research Associate Requirements:

• Bachelor’s degree in biological science or a related field.
• 2+ years of experience as a clinical research associate.
• Knowledge of the pharmaceutical industry, terminology, and practices.
• Knowledge of FDA regulations and their practical implementation.
• Strong verbal and written communication skills.
• Proficient computer skills.
• Proficient with Microsoft Office Word, Excel, and PowerPoint.
• Ability to manage and prioritize workload effectively.
• Available to travel extensively and on short notice, and ability to manage travel schedules, such as flight schedules.
• Valid driver’s license, proficient driving skills, own reliable transport, and up-to-date car insurance.

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Research Associate / Senior Associate Job Description

Research associate / senior associate duties & responsibilities.

To write an effective research associate / senior associate job description, begin by listing detailed duties, responsibilities and expectations. We have included research associate / senior associate job description templates that you can modify and use.

Sample responsibilities for this position include:

Research Associate / Senior Associate Qualifications

Qualifications for a job description may include education, certification, and experience.

Licensing or Certifications for Research Associate / Senior Associate

List any licenses or certifications required by the position: CCRA, AALAS, CPA, CCRP, CCRC, GCP, ACRP, CPR, ASR, ASCP

Education for Research Associate / Senior Associate

Typically a job would require a certain level of education.

Employers hiring for the research associate / senior associate job most commonly would prefer for their future employee to have a relevant degree such as Master's and University Degree in Education, Social Science, Design, Communication, Writing, Conducting, Science, Computer Science, Civil Engineering, Geographic Information Systems

Skills for Research Associate / Senior Associate

Desired skills for research associate / senior associate include:

Desired experience for research associate / senior associate includes:

Research Associate / Senior Associate Examples

• Microsoft Word (.docx) .DOCX
• PDF Document (.pdf) .PDF
• Image File (.png) .PNG
• Routinely perform and assist with lung scaffold reseeding experiments
• Demonstrate excellent understanding of cGMPs and other relevant regulations
• Interface with cleaning staff, and Facilities/Operations to make sure the facility meets its intended use requirements to schedule routine cleaning and all the necessary calibration and preventive maintenance activities
• Support Formulation and Process Development group testing needs for projects in early and late stage development
• With supervision perform phase appropriate method qualifications and validations and execute transfer to other departments/sites
• With supervision lead small projects and work with other stakeholders
• Ability to troubleshoot and develop solutions to moderate problems
• Thoroughly make detailed observations, analyse data, interpret results and exercise appropriate technical judgment in the design, execution and interpretation of experiments
• Competent to assist in writing and reviewing of technical reports and SOPs
• Build relationships across team and other functions within the organisation
• Prior work analyzing complex biological samples
• Familiarity with standard bioinformatics tools like Python, Perl, or R
• Sterile cell culture technique
• Experience developing new chromatography or mass spectrometry methods
• At least four years of experience in FACS analysis and cell sorting, preferably in a FACS service lab
• A solid theoretical understanding of flow cytometry and fluorescent activated cell sorting, and the ability to explain and consult on these topics
• Assist in the development and documentation of appropriate standard operating procedures for conducting research on the effects of impulsive sounds (blast) on the middle ear
• Become accredited by the Council for Accreditation in Occupational Hearing Conservation (CAOHC)
• Assisting the Principal Investigators on volunteer participant recruiting, obtaining and documenting volunteer informed consent, conduct of research protocols and test plans, data analysis, and manuscript review
• Assisting the Acoustics Division investigators in maintaining the records required by the USAARL Regulatory Compliance Office
• Obtain USAARL research credentials as an Associate Investigator
• Learn the art and strategy of medical communication and marketing
• Work closely with medical directors, copywriters, and editors in a team environment
• Have the opportunity to go in-depth into a therapeutic category, work across other disease states, as needed
• Conduct in-depth research using scientific publications and clinical trials
• Translate complex scientific concepts and maintain the scientific integrity for all aspects of clinical data for a brand
• Preparation of DNA and RNA sequencing libraries for Illumina platforms
• Operation of laboratory robotics (e.g., Agilent Bravo, Tecan, Hamilton, Beckman)
• Experience with nucleic acid sample quantitation methods (Fragment Analyzer, Qubit, qPCR )
• Flexible, being able to respond quickly to shifting priorities
• BS/MS in Biology/Molecular Biology, Biochemistry, Chemistry or related discipline, PhD not required
• Pacific Biosciences ‘long read’ library prep
• Process tissues (mouse, non-human primate, or human origin) for staining
• Maintain culture of primary cells and cell lines
• Independently analyze and document results
• Present findings in a timely manner
• Creating detailed documentation for clients and team members in areas such as installation, instructions, troubleshooting guidelines
• Identifying needs not being met by current supported software, and researching new solutions to meet needs and solve operational problems
• Execute complex laboratory experiments without supervision and clearly report out results in a timely
• Assist in preparation and characterization of drug formulations
• Maintain specific laboratory equipment
• Maintain cell lines and perform cell-based assays
• Emphasis or coursework in acoustics highly desired
• Research experience desired
• Work experience requiring exceptional written and verbal communication skills
• Work experience using Microsoft Windows 7 operating system and office and analytical software as appropriate to the task
• Advanced in vivo skills such as small animal surgeries and experience with more complex xeno-transplantation models (eg
• University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution, nursing certification, medical or laboratory technology
• Develops, implements, and coordinates efforts to develop large proposals to the federal government
• Develops a rapport and credibility with appropriate parties to best facilitate engaging them in substantive research partnerships within the industry
• Understands and promotes the research capabilities and interests of the Institute in terms of industry needs and national priorities
• Establishes a resource network in the community, the nation, and the international arena to identify and cultivate partners
• Makes final recommendations to management, public/private sector representatives and external constituencies
• Assists university departments by providing information for operational and strategic plans, or accreditation reviews
• Develops and delivers presentations, writes articles and technical reports
• Conducting, collecting and analyzing participant evaluations and research data
• Developing professional development materials such as multimedia, webinars based on best practices and research outcomes
• Drafting reports of interview findings
• Experience with mammalian cell culture valued but not required
• Self-motivated with a “can-do” attitude is required for success
• Flexible, able to respond quickly to shifting priorities and able to multitask
• A Bachelor or Masters degree in microbiology, molecular biology, or genetics is required
• Organizational skills, attention to detail, ability to multi-task, intellectually flexible and excellent verbal/written interpersonal communication skills are required
• Maintain safety documentation according to lab protocols and applicable governmental regulations
• Serve as lead evaluator on complex evaluation projects
• Collect and analyze qualitative and quantitative data
• Prepare appropriate reports for various audiences and stakeholders including state policy makers and funders
• Organize and maintain project materials
• Work collaboratively with all evaluation team members
• Assist with sample preparation on the bench top and inside of a glovebox using traditional cutting and polishing methods advanced techniques including FIB, ion milling and coating deposition
• Perform characterization of materials including electron microscopy (FIB/SEM, TEM) and chemical analysis
• Interact with customers, assessing problems, and assisting in solving materials related problems
• Safely handle, store, and dispose of radioactive materials on a daily basis
• Experience in method development for HPLC and/or mass spectrometers
• Strong organizational skills, ability to multi-task and meet timelines are critical requirements of this position
• Demonstrated experimentation in molecular biology and biochemistry in particular assay development as it relates to nucleic acid biochemistry, and double strand break technology
• Working knowledge of high throughput next generation DNA sequencing technologies
• Basic computer competencies required
• A masters degree (B.A, B.S

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The Job Description of a Clinical Research Associate

Clinical research associates are also referred to as CRAs. They are responsible for organizing and administering clinical trials of a current or new drug to assess and determine the risks and the benefits associated with using them. Clinical research associates are often employed by clinical contract agencies and pharmaceutical companies. There are many things that a clinical research associate needs to handle, and we will discuss them in this article.

Their responsibilities

The key responsibilities that a clinical research associate has to carry out in their course of duty include:

 Writing reports

 Progress monitoring during the trial duration

 Collection and authentication of forms that are used for data collection

 Giving the clinicians instructions about how trials are to be conducted

 Designing different trial materials as well as providing different study centers that have sufficient quantities

 Setting up the trial centers and then disbanding them

 Identifying the clinicians and briefing them

 Writing down the procedures of the drug trials

The employers

Typical employers include:

 The academic departments in hospitals

 Clinical contract houses and agencies (CROs)

 Pharmaceutical companies

Available vacancies are usually advertised in the national newspapers, online, specialist agencies, and very specific journals. This field is very competitive, therefore it can be useful for applicants to have the relevant analytical and scientific techniques. In addition, pharmaceutical research, medical sales, nursing, or laboratory work knowledge can be very useful in clinical research associate positions.

The process of recruitment involves an interview, which is very technical. You will need to be trained to get the kind of qualifications that are necessary to excel in this area. To achieve this, you need to be qualified in life sciences or medical sciences. To learn more about clinical research professional courses, visit CCRPS .

Take courses from CCRPS and learn more on how to become a clinical research professional.

Discover more from Clinical Research Training | Certified Clinical Research Professionals Course

Different Categories of Clinical Research Jobs Available as Careers

Understanding the scope of clinical research and what it entails.

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Research Associate Job Description: The 2024 Guide

Creating an effective job description for a research associate is essential in attracting qualified candidates and setting clear expectations for the role. A well-written job description should accurately reflect the qualifications, desired skills and job responsibilities of a research associate while also showcasing your company’s values and mission. In this blog, let’s understand how a research associate job description plays a crucial role in establishing the foundation for successful hiring processes.

Table of Contents

Research Associate Job Description: Sections to Include

Here are essential sections to include in a job description for a research associate:

1. Company Overview 

The company overview briefly explains your organization, what it does, its values, history, and work culture. The main aim of crafting an effective and accurate company overview is to introduce potential candidates to your company. It also helps you attract candidates who align with the values and goals of your company.

ABC is dedicated to pushing the boundaries of knowledge and discovery across various industries. As a premier research firm, we specialize in research projects and delivering actionable insights to our clients. Our team of experienced researchers, analysts, and subject matter experts collaborates closely to address complex challenges and drive innovation. With a focus on quality, integrity, and excellence, we strive to provide our clients with the strategic intelligence they need to make informed decisions and stay ahead of the competition.

2. Research Associate Job Description

This section of your research associate position description provides a brief overview of the roles and responsibilities of a research associate. It should outline the primary duties of a research associate within your company. 

As a Research Associate at ABC, you will play a key role in supporting our research initiatives and contributing to the development of innovative solutions for our clients. You will work closely with senior researchers and project managers to execute research projects, analyze data, and deliver actionable insights. This position offers a unique opportunity to gain hands-on experience in market research and make a meaningful impact on our clients’ success.

3. Research Associate Duties and Responsibilities 

This part of the job description for a research associate includes an in-depth explanation of the duties and obligations necessary for the role of a research associate. This should encompass all relevant tasks and research associate responsibilities that meet your organization’s requirements.

• Assist in designing research methodologies and data collection strategies.
• Conduct literature reviews and gather relevant secondary research data.
• Collect and analyze primary research data through surveys, interviews, and focus groups.
• Use statistical software to clean, analyze, and interpret quantitative data.
• Prepare research reports, presentations, and visualizations to communicate findings to clients.
• Collaborate with cross-functional teams to ensure research projects are executed efficiently and meet deadlines.
• Stay current with industry trends and best practices in market research methodology.
• Support business development efforts by contributing to proposal writing and client presentations.
• Participate in internal knowledge-sharing activities and contribute to the continuous improvement of research processes.

4. Research Associate Qualifications & Skills 

To effectively attract suitable applicants, it is crucial to clearly outline the necessary qualifications and skills required for success in the research associate job profile within your organization. This will effectively streamline your recruiting process and attract only qualified talent who possess the right skills.

• Bachelor’s degree in mathematics, business, economics, psychology, or related field (Master’s degree preferred).
• 1-3 years of experience in market research or related fields.
• Proficiency in quantitative and qualitative research methods.
• Strong analytical skills and attention to detail.
• Excellent written and verbal communication skills.
• Ability to work independently and collaboratively in a fast-paced environment.
• Proficiency in statistical analysis software, such as SPSS, SAS, or R is a plus.
• Knowledge of data visualization tools, such as Tableau or Power BI is a plus.

5. Salary & Benefits

It is important to include details on the compensation package in your research associate job profile as well as any additional bonuses or advantages offered. Also, highlight any distinctive perks or rewards that make your organization stand out and demonstrate your commitment to employee satisfaction.

Offered CTC: ₹5 LPA to ₹7.8 LPA

• Competitive salary
• Health, dental, and vision insurance coverage
• Retirement savings plan 
• Paid time off 
• Professional development opportunities
• Collaborative and inclusive work environment

The call-to-action section of a job listing is essential for encouraging interested individuals to apply for the role. Be sure to provide clear and concise instructions on how candidates can submit their applications for the research associate job profile.

How to Apply?

To apply for the Research Associate position at ABC, please submit your resume and cover letter detailing your qualifications and interest in the role to [email protected]. We look forward to reviewing your application and discussing how you can contribute to our dynamic team.

Research Associate Job Description Template

Below is a ready-to-use sample of a research associate job description outlining all the roles and responsibilities of a research associate.

Creating an effective job description for a research associate is important in attracting the right candidates and ensuring the success of your organization. A well-written job description should clearly outline the responsibilities, qualifications, and expectations of the role while also showcasing your company’s values and culture. This will not only help you find suitable candidates but also set them up for success by providing clear guidelines on what is expected from them. 

Hire talent from Internshala by posting your job description for free. Also, check out this guide on the top 10 recruitment strategies to hire the best employees.

Answer: Some major responsibilities of a research associate are: – Oversee the advancement of research projects and facilitate communication among different departments.  – Conduct diverse and complex tests and investigations.  – Execute specialized and advanced experiments.  – Gather, prepare, examine, and assess results.

Answer: Applicants must hold a Ph.D. in either science or engineering, an MD/MS/MDS in medical science, or an ME/MTech/MPharm/MVSc and have at least three years of R&D experience.

Answer: It typically takes 1-2 years to qualify as a Research Associate, while becoming a Researcher usually requires 2-4 years.

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Senior Clinical Research Associate Job Description, Key Duties and Responsibilities

This post provides detailed information on the senior clinical research associate job description, including the key duties, tasks, and responsibilities they commonly perform.

It also highlights the major requirements you would be expected to fulfill to be hired for the senior clinical research associate role.

What Does a Senior Clinical Research Associate Do?

A senior clinical research associate (CRA) plays a critical role in the planning and execution of clinical trials to test medical treatments and drugs.

The senior clinical research associate job description involves overseeing and managing clinical trials at medical facilities and research sites.

It also entails ensuring that activities adhere to established protocols, guidelines, and regulations.

Senior clinical research associates may directly supervise teams of CRAs and other site personnel involved in trials.

They typically report to the clinical operations manager or director.

Most positions are office-based, but frequent travel is required to visit research sites across the country or globe. Overnight stays near trial sites last weeks or months.

They require a Bachelor’s degree in science/health; higher education like a Master’s degree or RN is preferred.

Relevant experience in clinical trials or research is mandatory.

The core duties of a senior clinical research associate include project management and monitoring of trial timelines, budgets, drug supply chains, data quality, and site performance.

They are also responsible for identifying and troubleshooting any issue.

Other responsibilities they perform can include training site staff, writing reports, submitting documentation to regulatory agencies, and ensuring ethics committee approval.

This role is critical in countries with major pharmaceutical industries driving clinical trials globally.

Employers usually seek detail-oriented candidates with leadership abilities for the senior clinical research associate role.

Positions in the USA require certification from associations like ACRP; other countries have similar requirements. Regulations govern each step of the trials process.

The high level of coordination and troubleshooting makes the senior CRA integral to successfully completing clinical trials.

Next, we’ll look at some specific examples of tasks senior clinical research associates carry out:

Senior Clinical Research Associate Job Description Example/Sample/Template

The senior clinical research associate job description commonly consists of the following duties, tasks, and responsibilities:

• Develop detailed project plans and budgets for clinical trial protocols; oversee and track progress to timelines
• Lead training initiatives and onboarding of research staff at trial sites; provide ongoing support and education
• Create master drug supply forecasts and manage distribution logistics to trial locations
• Conduct on-site and remote monitoring visits of trial locations to review regulatory documentation, drug storage procedures, equipment calibrations, etc. Identify any deficiencies or training issues
• Monitor patient recruitment and enrollment numbers; recommend and assist with recruitment strategies to meet targets
• Review complex datasets and information from trial sites related to safety and efficacy; ensure accuracy and completeness
• Write visits reports, summaries, and other central documents to capture key trial information for lead scientists and regulatory submissions
• Serve as main point of contact for questions, issues, or feedback from site personnel; provide guidance and leadership 
• Track site performance benchmarks and metrics related to enrollment, data quality, protocol adherence
• Develop solutions for operational challenges that arise; adjust plans to minimize impact on trial execution 
• Ensure ethical guidelines, safety regulations, and GCP principles are strictly followed across all trial locations
• Represent trials and sponsor companies at investigator meetings, conferences, trainings, etc.
• Lead or assist sponsor companies with final analysis, evaluation, and conclusions of trial data
• Prepare sites and systems for regulatory inspections; may participate or present in inspections
• Maintain expert level knowledge on regulations, guidelines, systems in area of medical trials
• Communicate status updates, risks, final reports to leadership and key trial stakeholders 
• Develop data validation plans and quality control processes for trial data and systems
• Author SOPs, process documents, and training materials for trial sites and CRA teams
• Perform quality assurance audits on CRA monitoring activities and site performance
• Create agendas, content, and presentations for investigator meetings
• Compile data and generate reports for Data Safety Monitoring Board reviews
• Assist medical writing teams with clinical study report development
• Respond to inquiries from regulatory authorities regarding trial documentation and processes
• Liaise between sponsor companies and central lab facilities coordinating sample analysis 
• Develop contingency plans for trial delays, enrollment issues, site staffing problems etc.
• Create newsletters, status communications to inform trial leadership and stakeholders
• Conduct benchmarking studies on site metrics from past trials to set performance targets
• Review CRA monitoring plans and travel itineraries to provide oversight and optimization
• Analyze site contracts, agreements, and budgets during trial planning and initiation
• Assist with design and evaluation of case report forms, data capture tools, and eCRF components
• Develop transition plans for handoff of trials monitoring activities from remote to on-site visits.

Senior Clinical Research Associate Job Description for Resume

If you have worked before as a senior clinical research associate or currently working in that role and are making a new resume or CV, then you can create a compelling Professional Experience section for your resume by applying the sample senior clinical research associate job description provided above.

You can highlight the duties and responsibilities you have performed or are presently carrying out as a senior clinical research associate in your resume’s Professional Experience by utilizing the ones in the senior clinical research associate job description example above.

This will show that you have been successful performing the senior clinical research associate duties, which can boost your chances of being hired, especially if the new job that you are seeking requires someone with some senior clinical research associate work experience.

Senior Clinical Research Associate Requirements: Skills, Knowledge, and Abilities for Career Success

Here are important requirements that candidates for the senior clinical research associate role may be expected to meet to be hired:

• Expert knowledge of FDA regulations, ICH guidelines, GCP principles, and other standards related to clinical trials
• Leadership skills to manage teams, provide excellent customer service to sites, and troubleshoot complex issues
• Outstanding project management abilities to coordinate many trial details and juggle timelines
• Meticulous attention to detail regarding data, documentation, protocols, etc.
• Excellent written and verbal communication skills for drafting summaries, reports, emails, etc. to various stakeholders
• Strong analytical and critical thinking skills to analyze data, reports, processes and find potential improvements 
• Proficiency with key software platforms for clinical trials like EDC programs, CTMS tools, and eTMF systems
• Ability to exercise independent judgment when making recommendations and decisions impacting trials
• Skills in clinical knowledge, medicine, physiology, and related scientific fields 
• Fluency and literacy in interpreting medical and clinical trial documentation
• Proficiency in CDC principles of Good Clinical Practice
• Excellent organization skills to manage multiple priorities and deadlines
• Ability to maintain compliance across all trial systems and documentation
• Willingness and ability to travel frequently to sites across the globe. May require international travel logistics expertise. 

The senior CRA position combines project oversight skills with keen attention to scientific and regulatory details – not an easy mix of abilities! Employers highly value candidates who already have these competencies.

Senior Clinical Research Associate Salary

The median annual salary for senior clinical research associates in the United States was $126,837 in May 2022, according to the U.S. Bureau of Labor Statistics (BLS).

The top 5 paying states for senior clinical research associates in 2022 were:

• California: $156,335
• Massachusetts: $145,450
• New Jersey: $143,500
• New York: $142,390
• Connecticut: $141,890.

A senior clinical research associate plays an integral role in the complex world of clinical trials required to bring new medicines, devices, and treatments to market.

Their job description involves overseeing the operational side of trials to progress research from laboratories to patient bedsides as safely and efficiently as possible.

As we’ve explored, core duties focus on project leadership, research site management, budget and timeline tracking, and coordinated troubleshooting so data collection stays on track.

Senior CRAs combine scientific backgrounds with sharp project oversight abilities. 

Strong regulations mandate that patient rights, privacy, informed consent, and safety are protected during medical research.

Senior CRAs constantly ensure ethics and protocols are followed at all research sites under their responsibility.

This varied and demanding job provides an opportunity to facilitate life-changing medical discoveries while enjoying excellent salary growth and job prospects.

Candidates with the right balance of clinical knowledge, leadership talents, attention to detail and communication abilities are highly valued by research sponsors and organizations.

Hopefully, this guide provides helpful perspective both for aspiring senior CRAs as well as hiring managers looking to build standout teams for medical research programs that aim to significantly improve patient outcomes and standard of care.

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Clinical Research Coordinator Associate

🔍 school of medicine, stanford, california, united states.

The Division of Cardiovascular Medicine , within Stanford University Department of Medicine, is a dynamic and innovative center dedicated to excellence in research, medical education, and clinical care. Our Division is driven by over 90 faculty members and a cadre of staff who are the pillar of strength in the Division's ongoing efforts into the prevention and treatment of cardiovascular disease.

We are seeking a Clinical Research Coordinator Associate (CRCA) who is passionate about clinical research and wants to deliver results. The CRCA will work with a robust clinical research team, hand in hand with Principal Investigators, Clinical Research Managers, Associates and other stakeholders in support of patients with lymphedema and other lymphatic disorders.

The Clinical Research Coordinator Associate will be responsible for the overall implementation of an assigned set of research protocols assuring efficiency and regulatory compliance. Other responsibilities will include recruiting, screening, assisting in the informed consent process and enrolling subjects in accordance with good clinical practice guidelines as well as collecting, recording and maintaining complete data files using good clinical practice in accordance with HIPAA regulations. The CRCA will participate in data retrieval, reporting, and preparation of files and Case Report Forms for the various studies. Other duties may include processing of blood samples, reporting serious adverse events and maintenance of drug accountability, supplies and equipment.

CV Med Clinical Research is a growing, dynamic team who is dedicated to supporting translational medicine and contributing to Stanford Medicine’s mission. If you are eager to quickly achieve lasting results, we invite you to join our team!

Duties include:

• Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through close-out.
• Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment strategies.
• Collect and manage patient and laboratory data for clinical research projects. Manage research project databases, develop flow sheets and other study related documents, and complete study documents/case report forms.
• Ensure compliance with research protocols, and review and audit case report forms for completion and accuracy with source documents. Prepare regulatory submissions, and ensure Institutional Review Board renewals are completed.
• Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact.
• Monitor expenditures and adherence to study budgets and resolve billing issues in collaboration with finance and/or management staff.
• Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct.
• Ensure essential documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements.
• Participate in monitor visits and regulatory audits.

DESIRED QUALIFICATIONS:

• Bachelor's degree in a related field or an equivalent combination of related education and relevant experience; additional 1-2 years clinical trial experience preferred.

EDUCATION & EXPERIENCE (REQUIRED):

• Two year college degree and two years related work experience or a Bachelor’s degree in a related field or an equivalent combination of related education and relevant experience.

KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED):

• Strong interpersonal skills.
• Proficiency with Microsoft Office.
• Knowledge of medical terminology.

CERTIFICATIONS & LICENSES:

• Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred.

PHYSICAL REQUIREMENTS:

• Frequently stand, walk, twist, bend, stoop, squat and use fine light/fine grasping.
• Occasionally sit, reach above shoulders, perform desk based computer tasks, use a telephone and write by hand, lift, carry, push, and pull objects that weigh up to 40 pounds.
• Rarely kneel, crawl, climb ladders, grasp forcefully, sort and file paperwork or parts, rarely lift, carry, push, and pull objects that weigh 40 pounds or more.

WORKING CONDITIONS:

• Position may at times require the employee to work with or be in areas where hazardous materials and/or exposure to chemicals, blood, body fluid or tissues and risk of exposure to contagious diseases and infections.
• May require extended or unusual work hours based on research requirements and business needs.
• Will be working at three different locations; Stanford Boswell Clinics, Portola Valley, and Santa Clara sites

WORK STANDARDS:

• Interpersonal Skills: Demonstrates the ability to work well with Stanford colleagues and clients and with external organizations.
• Promote Culture of Safety: Demonstrates commitment to personal responsibility and value for safety; communicates safety concerns; uses and promotes safe behaviors based on training and lessons learned.
• Subject to and expected to comply with all applicable University policies and procedures, including but not limited to the personnel policies and other policies found in the University's Administrative Guide,  http://adminguide.stanford.edu .

The expected pay range for this position is $31.73 to $36.54 per hour.

Stanford University provides pay ranges representing its good faith estimate of what the university reasonably expects to pay for a position. The pay offered to a selected candidate will be determined based on factors such as (but not limited to) the scope and responsibilities of the position, the qualifications of the selected candidate, departmental budget availability, internal equity, geographic location and external market pay for comparable jobs.

At Stanford University, base pay represents only one aspect of the comprehensive rewards package. The Cardinal at Work website provides detailed information on Stanford’s extensive range of benefits and rewards offered to employees. Specifics about the rewards package for this position may be discussed during the hiring process.

Why Stanford is for You Imagine a world without search engines or social platforms. Consider lives saved through first-ever organ transplants and research to cure illnesses. Stanford University has revolutionized the way we live and enrich the world. Supporting this mission is our diverse and dedicated 17,000 staff. We seek talent driven to impact the future of our legacy. Our culture and unique perks empower you with:

• Freedom to grow . We offer career development programs, tuition reimbursement, or audit a course. Join a TedTalk, film screening, or listen to a renowned author or global leader speak.
• A caring culture . We provide superb retirement plans, generous time-off, and family care resources.
• A healthier you . Climb our rock wall, or choose from hundreds of health or fitness classes at our world-class exercise facilities. We also provide excellent health care benefits.
• Discovery and fun . Stroll through historic sculptures, trails, and museums. 
• Enviable resources . Enjoy free commuter programs, ridesharing incentives, discounts and more.

The job duties listed are typical examples of work performed by positions in this job classification and are not designed to contain or be interpreted as a comprehensive inventory of all duties, tasks, and responsibilities. Specific duties and responsibilities may vary depending on department or program needs without changing the general nature and scope of the job or level of responsibility. Employees may also perform other duties as assigned.

Consistent with its obligations under the law, the University will provide reasonable accommodations to applicants and employees with disabilities. Applicants requiring a reasonable accommodation for any part of the application or hiring process should contact Stanford University Human Resources at [email protected]. For all other inquiries, please submit a contact form .

Stanford is an equal employment opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.

• Schedule: Full-time
• Job Code: 1013
• Employee Status: Regular
• Requisition ID: 102959
• Work Arrangement : On Site

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MEDICAL RESEARCH ASSOCIATE JOB DESCRIPTION

Find detail information about medical research associate job description, duty and skills required for medical research associate position.

What do you do as a research associate?

Eva is a research associate at a consulting firm. She specializes in market research and economic analysis. Eva has a wealth of experience in both private and public organizations. Her skills help her to plan and conduct research on topics that are important to her clients. Eva is an expert in the field of economic analysis, and her work contributes to the success of her consulting firm.

What are the jobs of a CRA?

A CRA is responsible for monitoring study sites and clinical activities, updating study documentation, maintaining clinical data systems and coordinating research procedures. A CRA is also responsible for providing support to researchers in the process of conducting their studies.

Is a research associate a doctor?

A research associate is someone who helps researchers by playing a role in their work. They have a graduate degree, and are often in a position to help with the research itself as well as provide support when needed.

Is CRA a good career?

A career in certified research accounting would be a great choice for someone looking to make a big impact in the world. CRA is a highly respected profession with many years of experience, and they can earn a good salary and have a lot of opportunities to contribute to their work.

Is research associate job permanent?

A Research Associate is a budgeted position with a formal job description that is perpetual in an academic institution. A Research Fellow, on the other hand, is a limited-term appointment that is normally funded by an endowment or research grant from a state, federal or private company. A Research Associate brings years of experience and knowledge to the table as they work with researchers and professors to help carry out their research goals. They are responsible for managing research budgets and ensuring the success of their projects. Furthermore, they are also expected to work closely with other team members in order to achieve common goals and objectives.

How do I prepare for a research associate interview?

"I am interested in working as a research assistant because I want to learn more about different cultures and their customs. I also believe that this position will allow me to gain experience in a variety of fields. My long-term career goals include working for an organization that is dedicated to helping people." - source.

What is a clinical research associate salary?

Clinical Research Associates (CRA) are a vital part of any medical practice and can often offer high salaries for their work. In India, CRA salaries range from ? 1.9 Lakhs to ? 7.1 Lakhs with an average annual salary of ? 3.6 Lakhs. This is a great opportunity for those looking to rise up the career ladder and make a significant impact in their field.

How do I become a CRA?

Looking for a challenging, yet rewarding job? Look no further than the AcrpOptions program! They offer individuals a complete 3,000 hours of essential job duties or 1,500 hours of equivalent work experience requirements through the certifications or approved clinical research degree programs accredited by the Council for Higher Education. With the unique approach to training, you'll be able to develop your skills and knowledge in areas such as business administration, social media management, and more. Plus, the team is passionate about helping people succeed and we're always looking for talented individuals to join the team. So if you're interested in learning more about what AcrpOptions has to offer, please send us your resume and we'll be happy to look into it!

Why do you want to become a clinical research associate?

It can be difficult to choose the right career for someone, especially if they've never worked in a specific field. However, there are many opportunities out there for those who are willing to take on a new challenge. If you enjoy variety and want to be challenged, then a career in research is the perfect choice for you. Not only do you have the opportunity to work in different areas of research, but you also have the opportunity to write reports, go into meetings and get to know hundreds of different people.

What is the difference between CRA and CRC?

A CRA is a requirement for many jobs in the workforce, such as in research. A CRC, on the other hand, is most often used by people who have only a high school diploma or less. This difference can make a big difference in the amount of experience someone has when it comes to job hunting and finding a career.

What is the difference between research assistant and research associate?

An experienced research associate can be a great help to a professor in their research project. They have the ability to take on many tasks, from data collection to analyzing the data. Research assistants typically have a higher level of experience than a research associate, but they are still required to follow directions and meet deadlines.

What do research assistants in hospitals do?

Clinical research assistants are responsible for identifying subjects or clinical trials, collecting data, Evaluating results, and taking notes on activities in order to conduct scientific studies. They can also be used in other settings such as hospitals, laboratories, and other institutions. Clinical research assistants are essential for the success of scientific studies and can lead to important Discoveries.

Is CRA job stressful?

When you reach your one year as a CRA, it feels like it's such a stressful rollercoaster. Even when you're on vacation or sick, you can't help but think about all the work that still needs to be done. Your body is feeling the stress. That's because there are always so many things to worry about and keep track of. It can be hard to stay focused on your goals when everything else around you is constantly pushing you in different directions. However, by taking some time for yourself and setting aside some time each week to focus on your CRA goals, you can slowly start to feel better. This will help you relax and enjoy your time off while still ensuring that all of your important tasks are completed successfully.

What can I do after clinical research associate?

If you're interested in pursuing a career in clinical research, you may want to consider starting off your career as a Clinical Research Associate (CRAS). CRASes work within the clinical research field and are responsible for managing and conducting clinical trials. They can also be an important part of the Scientific Committee that approves research projects.

How much vacation do CRA employees get?

Parks and Recreation fans rejoice! Your vacation entitlement increases every year you work for the same employer. After 5 consecutive years of employment, you are entitled to 3 weeks of vacation. After 10 completed years, employees are entitled to 4 weeks of vacation.

Can you be a research associate without a PhD?

Anna is a research fellow at the University of Utah. She has a PhD in neuroscience from Cambridge, England. Anna is well-known for her groundbreaking research in the area of synaptic plasticity, which has helped her become one of the most respected scientists in her field. Her work has also been instrumental in developing new treatments for diseases such as addiction and schizophrenia.

What experience do you need to be a research assistant?

Looking for a challenging and rewarding job? Look no further than an English assistant position! As an assistant, you will be responsible for helping professionals write and improve their writing skills. In addition to providing support, you will also have the opportunity to learn new techniques and strategies. If you are interested in a career in writing, then an English assistant position is the perfect place for you!

Do you need a Masters to be a research assistant?

Most Research Assistant positions are responsible for providing support to scientific researchers by carrying out various tasks such as data entry, data analysis, and writing reports. Research Assistant jobs can be found all over the world, and they can provide a great opportunity for someone with an undergraduate degree to gain experience in a professional setting. In most cases, Research Assistant jobs require only basic academic qualifications such as a undergraduate degree. However, some positions may require postgraduate qualifications such as a master's degree. Whatever your level of experience, it's important to have the right skills in order to take on a Research Assistant job. Here are some tips to help you get started:

How many questions are asked in a research interview?

A recent study found that the number of questions needed for a perfect test is between 5 and 10. This means that if you want to pass your test, you need to know at least a few questions.

What skills are required for a clinical research associate?

A CRA is a professional who helps organizations by conducting research. They need to have excellent organizational skills, be able to work well with others, and be able to document and record tasks. They also need to be able to communicate effectively with people.

What questions are asked in a research interview?

No one knows what the future holds, but with the right planning and dedication, anyone can achieve success. In research, you'll use your knowledge and skills to find new ways to improve the products and services. This is a difficult process, but with hard work and determination, you can make a real impact on society.

How can I become a medical researcher after 12th?

Medical researchers are responsible for conducting research in order to improve the health of people. They use their scientific skills to analyze data and find solutions to problems. One of the most important skills a medical researcher needs is critical thinking. To be successful in this job, you must be able to think critically and come up with ideas for solving problems. Another important skill a medical researcher needs is research. You must be able to do research in order to learn about different diseases and how they can be treated. Finally, you must have good observational skills in order to see what is happening in the world around you and make informed decisions about how to improve the health of people.

What is the qualification for clinical research?

A diploma in clinical research is a 1-year course that provides the necessary skills for working in the medical field. With a 55 per cent score in graduation from medical science courses, or a degree in Pharmacology, Science, Pharmacy, Biotechnology, Life Sciences, etc., you are well on your way to becoming a successful doctor.

What is the highest paying job in clinical research?

There are many opportunities for career growth in the clinical research field. These jobs can offer great pay and a good work/life balance. Clinical Research Physicians, Laboratory Directors, and Project Managers are all in high demand, and can make a significant impact on the success of clinical trials. The salary range for these positions is from $191,000 to $269,500 per year. The most desirable position for a Clinical Research Manager is the Regional Clinical Research Associate. This position offers great pay and excellent benefits, as well as the opportunity to work in a very supportive environment.

How much is CRA training?

A Clinical Research Associate (CRA) is a position that provides critical oversight of clinical trials. They may work directly with the sponsor company of a clinical trial, or for a Contract Research Organization (CRO). CRA's responsibilities include monitoring the study's progress, and acting as an independent freelancer or for a trial sponsor that they are contracted to.

How do I get into medical research without experience?

Looking to get involved in Clinical Research? There are many ways to get experience, and one of the best ways is through volunteering at a healthcare company, clinician or research site. interning at a government agency can be an excellent option as well. In addition, there are many clinical research sites and organizations that offer volunteer opportunities, so it?s important to check out what options are available before making a decision.

Is clinical research a good job?

Most clinical trials are conducted in order to find a new cure or treatment for a specific disease. This research is often difficult and time-consuming, but it is a necessary part of medical progress. The global clinical trials market is expected to grow significantly over the next few years, as new vaccines and therapeutics become available.

Does clinical research pay well?

Clinical research associates (CRA) work in a variety of positions in the research field. They may be working as scientists or engineers, but all CRA have one common goal: to help others by contributing their knowledge and skills. In order to make a living as a CRA, many people must take on multiple jobs in order to make ends meet. The median salary for an entry-level CRA job is $64,519, while the median salary for a senior CRA job is around $133,552. This means that even if you?re not the best at everything, you can make a decent living as a CRA.

Why is a CRA important?

It is the responsibility of the Canadian Researchers? Association (CRA) to monitor a clinical trial, which includes that the rights and well-being of human subjects are protected, the reported trial data are accurate, complete, and verifiable from source documents. The conduct of the trial is in compliance with the currently approved protocol.

Is clinical research associate higher than coordinator?

Clinical research associates (CRA) manage multiple trial sites at one time and have a bachelors degree. They are usually paid more than coordinators, which is why they play an important role in clinical trials. CRAs produce outcomes that are cost-effective for improving the efficiency of a trial.

Can a CRC become a CRA?

CRC has a great deal of experience in writing creative English. This ensures that their clients receive the best possible writing service. CRC's Certifications and Tests ensure that their clients are fully prepared for any writing project they may face.

How do you move up in clinical research?

A Clinical Trials Manager's Top Tips for Starting and Mid-Level Careers in Clinical Research There are many ways to pursue a career in clinical research. One way to start is by volunteering at a hospital or research institute. You can also start small and aim high, by highlighting what you can bring to the position. Finally, be prepared to work long hours, asclinical research is a demanding field.

Is research associate higher than research analyst?

An associate professor at a university is a position that is lower in rank than an analyst but higher in rank than a writer. Associate professors teach undergraduate courses and may also teach graduate courses. They are not as involved in research as analysts, but they do have a responsibility to help out their colleagues and the university.

Is assistant higher than associate?

If you're looking for a career in creative writing, there are many options available. Assistant jobs may be a good starting point if you're not sure what else to look into. Assistant jobs can vary in their responsibilities, but they all share one important task: to help the manager of a business run their business effectively.

What is a medical research assistant?

A medical research assistant collects, records, and analyzes experimental data. They also maintain laboratory equipment and keep inventory. This position requires the ability to observe and analyze data quickly and accurately. The research assistant must possess analytical, technical, observational, and time-management skills.

Is a research assistant a researcher?

A research assistant, or RA, is a person employed, often on a temporary contract, by a university, a research institute or a privately held organization for the purpose of assisting in academic or private research. A research assistant is responsible for carrying out assigned tasks and working under the direct supervision of their supervisors. They are typically used in fields such as science and engineering, mathematics and computer science, business administration and law.

Do Cras have to travel?

The CRAs at the center review their enrollment, data entry and adherence to the protocol and relevant regulations. This position is a fast-paced, deadline-driven career. CRAs are responsible for ensuring that the patient population is treated optimally and meet all their medication goals. They work closely with other clinicians to ensure that treatments are given as prescribed, and that patients receive the most effective care possible.

Is Clinical Research Associate a stressful job?

Clinical research can be a daunting experience. It can be filled with unpredictable, long hours, and meager entry-level pay. For all of you masochists like me who are still reading, you must like pain. But, if you're serious about finding a career in clinical research, it's worth it. Clinical research is a great way to learn about new and innovative ways to treat patients. You can also make a lot of money doing this type of work.

How many people work CRA?

The CRA is a government organization that helps Canadians file taxes. It has over 42,000 employees and approximately 10,000 in headquarters and 32,000 in the regions. The CRA's mission is to help Canadians pay their taxes and to make sure they are compliant with the law.

What is the next step after CRA?

A clinical trial or clinical affairs manager may have a career path that includes management roles such as: Clinical trial or clinical affairs manager. Senior clinical trial or clinical Affairs Manager. Associate Director of Clinical Research.

Which job is best in clinical research?

There are many opportunities for careers in clinical research. Clinical research data specialists can work in a variety of industries, such as health care, pharmaceuticals, and agriculture. Clinical investigator or clinical researcher can work in a variety of fields, including medicine and health sciences. Research pharmacist can work in the pharmaceutical industry and help to create new medications. Clinical project manager can help to develop and lead clinical trials. Medical laboratory scientist can work with laboratories to study medical problems and diseases. Medical/scientific writer can write articles about scientific topics for publications. Marketing and communications professionals can help businesses communicate with their customers.

Is clinical research a good career in India?

Clinical research in India is a lucrative industry that offers great opportunities for researchers with the right skills and experience. The industry is growing rapidly and has potential to bring significant growth to the country. There are many talented researchers available in India, and projects that are started in this area can often lead to increased profits for companies and individuals involved.

Does CRA pay overtime?

A worker who receives a pay rate of at least 1.5 times the regular hourly wage, or time off with pay, equivalent to 1.5 hours of time off for every hour worked (for example, 5 hours of overtime worked = 7.5 hours of time off with pay) is entitled to a total amount of time off equal to the number of hours worked plus 1.5 times the regular hourly wage.

What holidays are paid in Canada?

Most people in Canada enjoy 10 paid holidays per year. These days are usually spent enjoying rest, relaxation, and some time with family and friends. This code of conduct provides for a few days off to reflect the country's values.

How many sick days do you get a year in Canada?

In September 2019, the Code also provides for up to five days of personal leave per year, three {3} paid and two {2} unpaid which are from now on not to be used for illness or injury. They currently have seven {7} personal days (that can be used for multiple reasons) and the Short-Term Disability Program (STDP). The ${7} personal days in 2019 are a great way to take some time for yourself, whether it's to recover from illness or injury, or justto relax. The ${3} paid and two unpaid days in 2019 are also great opportunities for rest and relaxation, as they help to avoid overuse of the ${2} unpaid day in 2019.

More jobs related with Medical

Biotech Research Associate

Job description overview.

A Biotech Research Associate job description involves working in the science industry, where the focus is on developing new drugs and medical technologies. A Biotech Research Associate works in a lab, assisting with experiments, analyzing data, and developing reports. This role typically requires a degree in science or a related field, and experience working in a laboratory setting. Biotech Research Associates are responsible for conducting experiments under the direction of their supervisors, ensuring that they follow established protocols and safety guidelines. They also assist with sample preparation, data collection, and analysis. Biotech Research Associates must be able to work independently, as well as part of a team. They must be detail-oriented, have strong problem-solving skills, and be able to communicate effectively. Overall, a Biotech Research Associate plays an essential role in the development of new drugs and medical technologies, ensuring the safety and effectiveness of these products.

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Table of contents, job duties and responsibilities.

• Conduct laboratory experiments to support research projects
• Record and analyze data accurately
• Maintain and operate laboratory equipment
• Prepare and maintain laboratory reagents, solutions, and samples
• Collaborate with research team members and communicate findings
• Follow standard operating procedures and safety guidelines
• Attend team meetings and contribute to project planning
• Stay up-to-date on relevant scientific research and technology advancements
• Manage and organize laboratory inventory and supplies
• Assist with writing research reports and/or scientific publications

Experience and Education Requirements

To get a job as a Biotech Research Associate in the Science industry, you generally need a Bachelor of Science degree in fields like Biology, Biochemistry, or Biotechnology. Having a Master's degree or a Ph.D. can give you a competitive advantage over other candidates, but it's not commonly required. Employers also look for candidates who have practical lab experience, such as internships, co-op programs, or previous work experience in a research lab. You should also have strong written and verbal communication skills, teamwork abilities, and be able to stay organized and focused on complex tasks. Becoming familiar with industry-specific software and equipment is also helpful.

Salary Range

A Biotech Research Associate is a key player in the Science industry, responsible for conducting research and developing new products in biotechnology. Biotech Research Associates earn between $40,000 and $100,000 per year in the United States, with an average salary of $65,149. However, it should be noted that salary range can vary depending on factors such as years of experience, level of education and specific subfield working on.

In other countries, Biotech Research Associate salaries can also vary. In Canada, the average salary for a Biotech Research Associate is CAD 52,266, while in the United Kingdom, it is approximately £27,857. Data shows that these salaries are also influenced by the area of specialization, industry and company size.

Sources: 

• Payscale: Biotech Research Associate Salary Range - https://www.payscale.com/research/US/Job=Biotech Research Associate/Salary 
• Glassdoor: Biotech Research Associate Salaries - https://www.glassdoor.com/Salaries/biotech-research-associate-salary-SRCH_KO0,27.htm 
• Indeed: Biotech Research Associate Average Salary - https://www.indeed.com/salaries/Biotech-Research-Associate-Salaries

Career Outlook

The career outlook for a Biotech Research Associate in the science industry over the next five years looks promising. The Bureau of Labor Statistics predicts that the employment in the life, physical, and social science occupations, which include biotech research, will grow by 5% from 2019 to 2029. This growth is due to the increasing demand for developing new drugs, technologies, and treatments for various diseases. With the COVID-19 pandemic, the importance of biotech research and development became even more apparent, and this will potentially boost job growth. Additionally, with the increasing investment in biotech companies and research, there will be more opportunities for biotech research associates to advance in their careers. Overall, the future for a biotech research associate looks bright.

Frequently Asked Questions (FAQ)

Q: What does a Biotech Research Associate do? 

A: A Biotech Research Associate is a scientist who conducts experiments and tests in a laboratory to support the development of new drugs, medical treatments, or technologies for the biotechnology industry. 

Q: What kind of education is required to become a Biotech Research Associate? 

A: A Biotech Research Associate typically needs a Bachelor's or higher degree in life sciences, biology, chemistry, or a related field. Some entry-level positions may only require an Associate’s degree or related experience. 

Q: What are the typical responsibilities of a Biotech Research Associate? 

A: A Biotech Research Associate is responsible for planning, conducting, and analyzing experiments using advanced laboratory techniques, ensuring experiments are done correctly and safety precautions are taken, documenting results in a clear and comprehensive manner, and assisting with the creation of reports and presentations. 

Q: What skills are important for a Biotech Research Associate? 

A: Strong attention to detail, ability to follow instructions accurately, excellent communication skills, ability to work well within a team, critical thinking skills to troubleshoot when experiments don't work, and knowledge of laboratory safety protocols are all important skills for a Biotech Research Associate. 

Q: What are some career opportunities for Biotech Research Associates? 

A: Biotech Research Associates can advance into positions such as Senior Research Associate, Research Scientist, or Project Manager. Biotech Research Associates can also move into other areas of the biotech industry, such as Quality Control, Manufacturing, or Regulatory Affairs.

Job Descriptions:

Clinical study manager, quality control specialist, medical writer, validation specialist.

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Postdoctoral Research Associate –Invasive fungal and bacterial diseases

Position Description

Supported by the Department of Energy Office of Biological and Environmental Research, this position will help develop a “Biopreparedness Research Virtual Environment” (BRaVE) platform to address current and emerging biothreats with an initial focus on the biomolecular characterization of a fungal disease targeting a bioenergy crop. The selected candidate will work as a part of a multi-disciplinary team to perform biomolecular characterization of plant-pathogen interactions through the utilization of integrated cell biology, biochemistry, structural biology, and bioimaging tools to investigate the pathogenic processes and the dynamics of infection, replication, release, and systemic transmission.  The integrated research will pave the way for early detection, characterization, and mitigation of emerging pathogens, creating a secure society and bioeconomy

This project will utilize the state-of-the-art BNL facilities NSLS-II on X-ray imaging and X-ray crystallography, CFN (Center for Functional Nanomaterials) and Biology Department on confocal light microscopy and live-cell imaging, LBMS on single-particle cryo-electron microscopy and cryoelectron tomography. NSLS-II is a world-leading synchrotron facility that produces high-flux, and low-emittance X-rays for solving a wide range of biological problems via diffraction, scattering, and imaging capabilities. CFN explores the unique properties of materials and processes at the nanoscale supported by the operation of high-end instruments from material fabrication and characterization to theory and computation. LBMS provides structure and imaging capabilities for studying biological structures and processes from near-atomic to nanometer resolutions. In addition, LBMS has an Aquilos 2 cryogenic focused ion beam (cryo-FIB) for cryo-electron tomography (cryo-ET) sample preparation and a high-pressure freezer for processing tissues and thick biological samples. The integrated BNL infrastructure will be an ideal environment for the project. This position has a high level of interaction with an international and multi-cultural scientific community.

Brookhaven National Laboratory and the Energy and Photon Sciences Directorate are committed to your success. We offer a supportive work environment and the resources necessary for you to succeed.

Essential Duties and Responsibilities:

• Prepare samples for downstream characterization. • Collect and analyze data. • Document experimental details and disseminate results through reports and publications.

Required Knowledge, Skills, and Abilities :

• Ph.D. in biophysics, molecular biology, biochemistry, chemistry, cell biology, plant biology, pathology, genetics, microbiology, immunology, virology, or a related field • Proven abilities for dissemination of research through publication in peer-reviewed journals

Preferred Knowledge, Skills, and Abilities:

• Experience in protein production from bacteria, insect, yeast, or mammalian cells • Experience in gene expression in plant leaves or protoplasts • Experience in protein crystallography • Experience in cryo-electron microscopy (single particle or tomography). • Experience in the use of a cryo-FIB for milling biological samples. • Experience in characterizing cells and tissues using live-cell imaging, X-ray tomography or X-ray fluorescence imaging. • Experience in the identification and characterization of protein-protein interactions using fluorescence, affinity purification, and Kd measurements. • Ability to communicate effectively and diplomatically. • Self-motivated and able to work both independently and as a team player.

Brookhaven Laboratory is committed to providing fair, equitable and competitive compensation. The full salary range for this position is $70200 - $90825 / year. Salary offers will be commensurate with the final candidate’s qualification, education and experience and considered with the internal peer group.

OTHER INFORMATION:

• Initial 2-year appointment subject to annual renewal contingent on performance and funding. Candidates should submit a CV, a brief description of their research interests (less than 200 words) in a cover letter and contact information for three references. • BNL policy requires that after obtaining a PhD, eligible candidates for research associate appointments may not exceed a combined total of 5 years of relevant work experience as a postdoc and/or in an R&D position, excluding time associated with family planning, military service, illness or other life-changing events.

Brookhaven employees are subject to restrictions related to participation in Foreign Government Talent Recruitment Programs, as defined and detailed in United States Department of Energy Order 486.1A. You will be asked to disclose any such participation at the time of hire for review by Brookhaven. The full text of the Order may be found at: https://www.directives.doe.gov/directives-documents/400-series/0486.1-BOrder-a/@@images/file

Equal Opportunity/Affirmative Action Employer

Brookhaven Science Associates is an equal opportunity employer that values inclusion and diversity at our Lab. We are committed to ensuring that all qualified applicants receive consideration for employment and will not be discriminated against on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, age, status as a veteran, disability or any other federal, state or local protected class. BSA takes affirmative action in support of its policy and to advance in employment individuals who are minorities, women, protected veterans, and individuals with disabilities. We ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

*VEVRAA Federal Contractor

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Laboratory and Research Associate - 128034

Job description, #128034 laboratory and research associate.

UCSD Layoff from Career Appointment : Apply by 02/09/2024 for consideration with preference for rehire. All layoff applicants should contact their Employment Advisor.

Special Selection Applicants : Apply by 02/22/2024. Eligible Special Selection clients should contact their Disability Counselor for assistance.

DESCRIPTION

The Department of Pediatrics is one of the largest departments within the School of Medicine with approximately 250 Faculty, 127 postdoctoral fellows (both MDs and PhDs) along with over 320 support staff (not including hospital staff). In addition, the Department has 68 clinical residents distributed across the Divisions. The missions of research, education, and patient care are intertwined and are integral to the goals of the department.

The Department has undergone significant growth in recent years with a consolidated budget of approximately $183 million including sponsored projects expenditures and clinical revenue. Expansion of the Department’s research and clinical portfolio is expected to continue in the next few years.

The Department’s 16 divisions include Academic General Pediatrics, Child Development & Community Health; Allergy, Immunology and Rheumatology; Cardiology; Dysmorphology; Emergency Medicine; Endocrinology; Gastroenterology; Genetics; Genome Information Sciences; Hospital Medicine; Host-Microbe Systems and Therapeutics; Infectious Diseases; Neonatology; Nephrology; and Respiratory Medicine.

In 2001, physicians and leadership of the University of California, San Diego (UCSD), Rady Children's, and Children's Specialists of San Diego (CSSD) unified pediatric patient care, research, education and community service programs, creating a university-affiliated children's health system to serve the region. Over the past two decades, an extensive list of joint programs has developed, with many physicians and researchers playing a role at both institutions.

This affiliation has consolidated the clinical, teaching, research, and public service programs of the UCSD School of Medicine's Department of Pediatrics with San Diego's only health care system dedicated to the health and well-being of children. In 2009, this partnership was furthered by the creation of Rady Children’s Specialists of San Diego, a Medical Foundation, and is now recognized as having global leaders in research, technology, translational medicine, education, and clinical excellence.

The multi-disciplinary lab within the Department of Pediatrics explores the roles of RNA biology in regenerative medicine and immune system regulation in cancer and host-pathogen interactions. Projects in the lab use cell culture, animal models, stem cells, human pluripotent cells, and several molecular tools to investigate fundamental mechanisms of cancer, COVID-19, AIDS, brain, and immune disorders.

Under supervision, the Research Associate will perform laboratory experiments such as RNAi and CRISPR gene editing in various cell lines and animal models, effect of various drugs on the brain, single cell RNA-Seq, ATAC-Seq, data generation, and analyses, preparation of reports and presentations.

MINIMUM QUALIFICATIONS

Theoretical and practical knowledge of life science such as biology, molecular biology, and biochemistry including relevant laboratory techniques as typically acquired through a Bachelors degree, or an equivalent combination of education and experience.

Experience performing high-level experimental and data analysis tasks.

Skill in and knowledge of operating and maintaining a variety of lab equipment.

Experience in maintaining well-organized lab and thorough records. Advanced math skills and ability to handle accounting and billing practices.

Demonstrated superior oral and written communication skills to communicate research results and carry out collaborative projects.

Ability to work under supervision and independently on projects with a variety of personalities.

Demonstrated ability to set priorities and to organize a varied workload to meet deadlines despite frequent interruptions.

Strong computer knowledge: Proficiency with Windows programs and knowledge of library usage with the willingness and ability to learn new hardware/software as required.

Knowledge of Cal-OSHA & UCSD EH&S safety requirements including MSDS's, hazard communication & Injury and Illness Prevention Program; laboratory safety precautions including appropriate clothing and shoes, use of protective items such as gloves and goggles as well as basic first aid procedures.

Ability to manage multiple projects, tasks and priorities to achieve desired goals.

Experience in conducting molecular experiments such as PCR, RNA, DNA assays.

Ability to use relevant computer software programs to organize and analyze data.

Skill and knowledge in maintaining cell culture facility.

Experience receiving and processing new samples of different cell lineages using standard repetitive protocols.

SPECIAL CONDITIONS

Employment is subject to a criminal background check.

Occasional evenings and weekends may be required.

Must be willing to work with hazardous materials.

Pay Transparency Act

Annual Full Pay Range: $58,548 - $94,190 (will be prorated if the appointment percentage is less than 100%)

Hourly Equivalent: $28.04 - $45.11

Factors in determining the appropriate compensation for a role include experience, skills, knowledge, abilities, education, licensure and certifications, and other business and organizational needs. The Hiring Pay Scale referenced in the job posting is the budgeted salary or hourly range that the University reasonably expects to pay for this position. The Annual Full Pay Range may be broader than what the University anticipates to pay for this position, based on internal equity, budget, and collective bargaining agreements (when applicable).

If employed by the University of California, you will be required to comply with our Policy on Vaccination Programs, which may be amended or revised from time to time. Federal, state, or local public health directives may impose additional requirements. If applicable, life-support certifications (BLS, NRP, ACLS, etc.) must include hands-on practice and in-person skills assessment; online-only certification is not acceptable.

UC San Diego Health Sciences is comprised of our School of Medicine, Skaggs School of Pharmacy and Pharmaceutical Sciences, The Herbert Wertheim School of Public Health and Human Longevity Science, and our Student Health and Well-Being Department. We have long been at the forefront of translational - or "bench-to-bedside" - research, transforming patient care through discovery and innovation leading to new drugs and technologies. Translational research is carried out every day in the hundreds of clinical trials of promising new therapies offered through UC San Diego Health, and in the drive of our researchers and clinician-scientists who are committed to having a significant impact on patient care. We invite you to join our team!

Applications/Resumes are accepted for current job openings only. For full consideration on any job, applications must be received prior to the initial closing date. If a job has an extended deadline, applications/resumes will be considered during the extension period; however, a job may be filled before the extended date is reached.

To foster the best possible working and learning environment, UC San Diego strives to cultivate a rich and diverse environment, inclusive and supportive of all students, faculty, staff and visitors. For more information, please visit UC San Diego Principles of Community .

UC San Diego is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age or protected veteran status.

For the University of California’s Affirmative Action Policy please visit: https://policy.ucop.edu/doc/4010393/PPSM-20 For the University of California’s Anti-Discrimination Policy, please visit: https://policy.ucop.edu/doc/1001004/Anti-Discrimination

UC San Diego is a smoke and tobacco free environment. Please visit smokefree.ucsd.edu for more information.

UC San Diego Health maintains a marijuana and drug free environment. Employees may be subject to drug screening.

Application Instructions

Please click on the link below to apply for this position. A new window will open and direct you to apply at our corporate careers page. We look forward to hearing from you!

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Posted : 4/18/2024

Job Reference # : 128034

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