clinical research associate vacancy

CRA Careers at IQVIA

Help tackle healthcare’s greatest challenges to improve patient health.

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Put your passion to work

IQVIA Clinical Research Associates play a vital role in the evolution of clinical development. They bring passion, ambition, and a deep level of expertise to help solve complex clinical issues while ensuring adherence to regulations and sponsor requirements. Here, you'll find the autonomy and flexibility you need to take your CRA career to the next level.

Choose your path

Sponsor-dedicated.

When you join as a sponsor-dedicated CRA, you’ll embrace the stability of a global contract research organization and harness the power of industry-leading technology. As part of this alignment, you'll gain valuable experience, working side by side one of our pharmaceutical customers, and expand your knowledge in a wide variety of therapeutic areas.

Our sponsor-dedicated model brings together the right people, experience and ideas to deliver high quality solutions specific to the customer’s needs.

Full-service

When you become a CRA as part of our full-service alignment, you'll embrace your passion for a specific therapeutic area and support a variety of sponsors. With access to world-class training and cutting-edge technology, developed specifically for IQVIA CRAs, you'll have the resources you need to create the career you want.

Our full-service model delivers cutting-edge clinical research through state-of-the-art innovation.

IQVIA Biotech

When you pursue a CRA career with IQVIA Biotech, you'll work directly with customers in a collaborative environment to help change the face of biotech. Using your extensive therapeutic knowledge, you’ll oversee uniquely-focused clinical studies, where you’ll be exposed to pioneering protocols and experience a dedicated partnership with your team like none other.

IQVIA Biotech is at the forefront of clinical trials in a variety of therapeutic areas through the delivery of flexible solutions within the biotech sector.

IQVIA empowers you to drive your own path within the organization. As no person's route is the same and the clinical research landscape is forever changing, you are encouraged to continually seek career growth opportunities and align your interests with your career goals.

Senior Clinical Research Associate 2

At IQVIA, we are committed to supplying our CRAs with the right tools, training and development support to allow for success and career growth. In addition to the rewarding work, collaboration and engaged line management, there is a constant focus on development as your career growth supports also the growth of the company.

Director, Clinical Operations

For me, it’s the people and knowing I’m making a difference in creating a healthier world that inspire me to come to work every day. I can go to anyone with a challenge, and they are willing to help. Together, we’re thinking outside of the box to navigate each sites’ unique needs and challenges.

Senior Clinical Research Associate

Explore unlimited opportunities

Clinical Research Associates can leverage their experience in a variety of ways that enable them to pursue their unique passions. Whether you choose to advance within a specific therapeutic area or want to explore something new, you can create the career you want. Explore the various career opportunities when you join IQVIA as a CRA.

What you can expect

All CRAs at IQVIA, regardless of alignment, thrive within our dynamic culture and experience:

Professional Development

Work-Life Balance

Supportive Leadership

Best-in-Class Training

Collaboration

Explore clinical monitoring jobs.

• R1414825 Sr CRA 1 Learn more Multiple Locations
• R1419171 2024 CRA DP Learn more Multiple Locations
• R1417873 CRA 2 Learn more Multiple Locations

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Clinical Research jobs

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Clinical Research Associate (CRA) careers in the USA with the FSP team at ICON

Apply for Clinical Research Associate (CRA) jobs with ICON, the world's largest provider of Functional Service Provision (FSP). We provide global strategic resourcing and FSP services to the biopharmaceutical and medical device industries. With more than 60 FSP solutions across all major functions from clinical monitoring and project management through data management, statistical programming now is a perfect time to join our team.

Why join the FSP team at ICON?

Working at ICON is more than a job, it’s a calling for people who care and are passionate about improving patients’ lives. At ICON, we care about our people and your passion, you are key to our success. We aim to provide an open and friendly work environment where we empower our people and provide them with opportunities to develop their long-term career.  

It takes courage to move from one job to another, the process involves careful consideration. Reach out having the conversation that would change your life and the lives of our patients. Our team of recruitment experts will provide the information you need in making the right decision.   

At ICON you will have the opportunity to work with one of the global top 20 pharmaceutical companies, working on novel therapies that deliver real impact. If you want a career with a difference, ICON is the place for you.

We have a range of job vacancies across the USA as well contract and homebased roles for experienced CRAs, CRA IIs and Senior CRAs.

CRA careers in US

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Employee stories

How can we help.

• Site & Patient Recruitment
• Medical Device
• Real World Evidence
• Decentralised & hybrid clinical trials
• Digital Disruption

Our single focus is the placement of quality CRAs and Site Managers

Why do companies choose cra resources as their cra service provider.

Extremely Low Attrition

Our tried and true processes will help you to minimize project disruption and cost

Choices: Never Settle

Our Clinical Research Associates will have the exact therapeutic experience you need to successfully monitor your studies

Speed to Market

Because CRA Staffing is our sole focus, h aving readily available quality monitors is typical for us as they roll off of other projects

A Clinical Research Associate (CRA) Recruitment Agency

craresources is a Niche Clinical Research Associate Recruiting firm, being truly unique in that placing CRAs and Site Managers is our sole focus.

We understand the impact Field Monitors have to the success or failure of your studies and because of this single focus, we are able to quickly and easily identify Field Monitors matching your therapeutic focus, experience requirements, and specific location needs while providing you with competitive compensation and rates.

With speed to market in mind, craresources provides best in class results by having our CRA Recruiters network strictly within the Clinical Research Associate community. We can accommodate your need for partial FTEs, a single FTE, or even several resources.

We also offer various pricing models such as hourly , per unit , or a flat fee for direct hire placement.

Our Vision: We deliver high quality CRAs to our Partners every time.

We believe clients should receive quality candidates every time.

LIKE YOU, WE ARE JUDGED BY RESULTS!

Is it time to consider a company with an excellent track record of effectively achieving Speed to Market while consistently delivering Excellence and Quality?

CRAs: Looking for New Consulting or Career Opportunities?

craresources recognizes that the skills and experience of our CRAs are our strongest asset. We work with the brightest and most talented Clinical Research Associates / Field Monitors in the industry and that is why many of the of the world’s leading pharmaceutical and biotechnology companies rely on us for their contract and permanent CRA Staffing needs.

Low on time?

Clinical research jobs.

At Proclinical Staffing, we are experts in recruiting for clinical research vacancies and are looking for experienced professionals for a broad and extensive range of positions across different company sizes and locations globally. Below, you will find our latest clinical research jobs in pharma, biotech, medical devices and in contract research organisations (CROs). We are recruiting for CRA jobs, Clinical Project Manager vacancies, and various other clinical operations and clinical development roles, right through to Clinical Director and VP Clinical Research in the US, across Europe, the UK, Switzerland, Australia and more. 

Use our life science job search  tool to refine the type of position or location you are looking for. Due to our strong partnerships with many of these companies, our vacancies are often exclusive, so you won't find them anywhere else.

Our recruitment consultants are experts when it comes to jobs in clinical research and when you send your CV to us , they will be able to match your profile with suitable positions when they become available. To be notified of clinical research vacancies that are tailored to your specific requirements, sign up for our job alerts!

Need help getting a clinical research job?

Take a look at our latest career advice articles for helpful tips from the experts or check out these articles for help advancing your clinical research career.

• Clinical research career paths - grow your clinical research career
• How to get a Clinical Research Associate (CRA) job
• How to progress from Clinical Trial Manager to Clinical Project Manager
• How to get a Clinical Project Manager (CPM) job
• 6 benefits of CROs for your clinical research career
• What Contract Research Organisations look for
• How to make your clinical research CV stand out

Latest jobs

Highly Competitive Salary

Paris, France

Proclinical is seeking a dedicated and experienced Clinical Research Director to manage the clinical activities of a range of products.

Highly Competitive

Philadelphia, USA

Proclinical is seeking a dedicated and organized Clinical Research Coordinator. This is a permanent position located in Philadelphia, PA.

City of London, England

Proclinical are seeking a dedicated Snr Clinical Trial/ Program Manager to accelerate the initiation within one of our London based biotech clients.

Brussels, Belgium

Proclinical Staffing are partnered exclusively with a start-up Biotech in Belgium who are looking for a well-seasoned Clinical Project Manager.

Broadway, USA

Proclinical is in search of a Phlebotomist for a leading CMO. This is a contract position located in Broadway, VA.

Proclinical is seeking a Clinical Research Nurse for a leading research institute. This permanent position is located in Philadelphia, PA.

New Haven, USA

Proclinical is seeking a Stability Sample Management Specialist for a leading pharmaceutical company. This is a contract position is located in New Haven, CT.

Proclinical is seeking a Professional Services Resource Manager. This role is pivotal in allocating resources to client projects.

Brussels, België

Proclinical are representing a medium sized, global biotech who are expanding rapidly due the significant products that are coming through in our clients pipeline.

Leiden, Nederland

Proclinical is seeking a Senior Clinical Scientist to join our team. This role is integral to our development organization as we prepare to start clinical development of our Axiomer pipeline.

Proclinical Staffing is seeking a Clinical Research Nurse to join a top medical program.

Detroit, USA

Proclinical Staffing is seeking a Clinical Research Oncology Nurse to join a top healthcare organization.

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Clinical Research Recruiting

Whether you are a Clinical Research professional looking for a new job opportunity; or aa Academic, Hospital based, Pharmaceutical, or Clinical Research Organization in need of quality Clinical Research professionals, you’ve come to the right place! We offer comprehensive recruitment services to Clinical Research professionals and organizations.

Please call us today at 469-246-4500 to start your search for your new Clinical Research job or candidate!

Upload your Resume for a Confidential Job Search

Submit a clinical research job order today.

Our Clinical Research  Recruiters  have extensive knowledge about Clinical Research sub-specialties and we listen to your desires and advise you about whether we can be helpful in your search. The majority of our recruiters are certified by the National Association of Personnel Services (NAPS) as Certified Personnel Consultants (CPC).

Nurse / Allied Health Recruiter

I have had the pleasure of working with one of your healthcare recruiters on several occasions. I have found her to be very easy to work with and a true professional in every sense of the word.

Practice Director Oncology Practice

I have worked with Odell Medical Search for the past several years. My experience has been very positive every time I have worked with Odell. I have worked with other agencies as well but found that the best candidates were the ones that Odell Medical Search located and brought to me. these candidates have also been long term employees and are still employed today.

Thank you so much for assisting us in our search for our Oncology Navigator Nurse Practitioner. With my personal background in Agency Recruitment, I have high expectations when dealing with search firms. I can tell you that Odell Medical Search met and exceeded all of my expectations. From the initial conference call to understand my need and the culture of our company to the thorough understanding of his candidates’ backgrounds and motivations, you truly did a wonderful job of finding the best candidate for our position. Odell was always timely with his follow up and had great “candidate control” throughout the process. It seemed like they were always a step ahead of me. Thank you again and I look forward to working with you in the future.

Below is a list of the different types of Clinical Research professional we are successful at placing:

• Oncology Clinical Research Nurse Coordinators
• Oncology Clinical Research Coordinators
• Regulatory Specialists/Coordinators
• Clinical Research Managers/Program Managers
• Clinical Research Supervisors
• Manager of Regulatory Compliance and Quality
• Clinical Data Coordinators
• Clinical Research Associates
• Manager of Clinical Research Business Operations
• Manager of Clinical Research Finance and Budgets
• Clinical Data Managers/Coordinators
• Director of Clinical Research
• Director of Regulatory Affairs
• Director of Research Finance
• Research Study Assistants
• Oncology Clinical Research
• Bone Marrow Transplant Clinical Research
• Car T-Cell Therapy Clinical Research
• Phase I Clinical Research
• Cardiology Clinical Research
• Cardiothoracic Surgery Clinical Research
• Cardiovascular Surgery Clinical Research
• TAVR Trans Aortic Valve Clinical Research
• LVAD Clinical Research Clinical Research
• Immunotherapy Clinical Research
• Electrophysiology Clinical Research
• ENT Clinical Research
• Gastroenterology Clinical Research
• General Surgery Clinical Research
• Gynecology Oncology Clinical Research
• Interventional Cardiology Clinical Research
• Neonatal Clinical Research
• Nephrology Clinical Research
• Neurology Clinical Research
• Orthopedic Clinical Research
• Perinatal Clinical Research
• Pediatric Clinical Research
• Radiation Oncology Clinical Research
• Urology Clinical Research
• Vascular Clinical Research

Clinical Research Resources

• ACRP – The Association of Clinical Research Professionals
• The Society of Clinical Research Associates (SOCRA)
• Society for Clinical Data Management (SCDM)
• Applied Clinical Trials
• CenterWatch: CLinical Trials Information

top resources

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Every day, our community of professionals is involved in mission-driven research around the globe, developing solutions to manage complex research in resource-limited settings. Explore current opportunities to work for FHI Clinical and support our global programs and operations. Your contribution will make a difference.

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Clinical Research Coordinator Associate (50% FTE/Fixed Term)

🔍 school of medicine, redwood city, california, united states.

The Department of Orthopaedic Surgery has an immediate opening for a Clinical Research Coordinator Associate (CRCA) fixed-term through December 15, 2024, part-time (50%) position to perform duties related to the coordination of clinical studies within the VOICES Health Policy Research Center. The VOICES Center is an active, growing health services research lab that focuses on shared decision making, defining quality for US and international orthopaedic care, improving value, reducing cost in healthcare, and eliciting patient preferences. The VOICES lab uses a variety of study designs, including qualitative research methods, clinical research, big data, chart reviews, systematic reviews, quality improvement initiatives, etc. to work towards the mission of the VOICES Center and the Department of Orthopaedic Surgery. To learn more about the Department please visit us at: https://ortho.stanford.edu/

The successful candidate will demonstrate:

• Outstanding communication and relationship building skills.
• Strong attention to detail, and competence to manage multiple priorities and respond effectively with limited guidance.
• Commitment to uphold Stanford University’s compliance with federal, state, local, and sponsor regulation.
• Drive to establish themselves as a leading contributor within the Department of Orthopaedic Surgery and Stanford Medicine.

Duties include:

• Serve as primary contact with research participants, sponsors, and regulatory agencies.  Coordinate studies from startup through close-out.
• Determine eligibility of and gather consent from study participants according to protocol.  Assist in developing recruitment strategies.
• Coordinate collection of study specimens and processing.
• 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. 

* - Other duties may also be assigned.

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.
• - Consistent with its obligations under the law, the University will provide reasonable accommodation to any employee with a disability who requires accommodation to perform the essential functions of his or her job.

WORKING CONDITIONS: 

Occasional evening and weekend hours.

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 $27.88 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 ( https://cardinalatwork.stanford.edu/benefits-rewards ) 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. 

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.

Consistent with its obligations under the law, the University will provide reasonable accommodation to any employee with a disability who requires accommodation to perform the essential functions of the job.

• Schedule: Part-time
• Job Code: 4924
• Employee Status: Fixed-Term
• Requisition ID: 102890
• Work Arrangement : Hybrid Eligible

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