clinical research coordinator jobs austin

Clinical Research Coordinator jobs in Austin, TX

Clinical Research Coordinator organizes research information for clinical projects. Selects and observes subjects and assists with data analysis and reporting. Being a Clinical Research Coordinator oversees experiment scheduling and collection of data. Requires a high school diploma or equivalent. Additionally, Clinical Research Coordinator typically reports to a supervisor or manager. The Clinical Research Coordinator works under moderate supervision. Gaining or has attained full proficiency in a specific area of discipline. To be a Clinical Research Coordinator typically requires 1-3 years of related experience. (Copyright 2024 Salary.com)

Recently Added Clinical Research Coordinator jobs

• TEXAS DIABETES & ENDOCRINOLOGY PA

Job Details

Description.

Texas Diabetes & Endocrinology, P.A. (TD&E) has grown over the years to meet the Endocrinology needs of the Austin community. Our mission is to strive to provide expert care in Diabetes, Thyroid problems, Osteoporosis, Weight management and hormonal conditions by providing thorough evaluations and innovative, personalized solutions focused on our patients success. Our employees are the strength that keeps us moving forward.

Our Clinical Research Department is looking for a Clinical Research Coordinator (CRC) I role at our Round Rock location!

While under 60-90% daily oversight of the Director/Assistant Director of Site Operations, the Clinical Research Coordinator (CRC) I is responsible for conducting and managing phase II-IV clinical trials while assuring protocol compliance. This position is also responsible for, but not limited to, overseeing the following: ensuring proper clinical trial protocol is completed at all times to obtain the correct data, collecting patient vitals during each visit, collecting data from pump/meters, working with providers to schedule updated patient checkup, keeping patient binders organized at all times, and communicating with sponsors with updates on patient data. The CRC I is also responsible for preparing written informed consent documents once the trial has been completed.

Key duties include but are not limited to:

• Manages clinical trials from start up to close out. Number of trials may vary depending on nature of study.
• Maintains a high level of knowledge and understanding of assigned protocols, including all protocol requirements for patient visits, obtaining informed consent, patient visit schedules, test procedures, laboratory information, and drug accountability requirements.
• Responsible for completion of all study documentation forms, including case report forms and other study specific documents.
• Assist Clinical Trial Recruiters/Assistant Clinical Research Coordinators (ACRCs) with recruitment and retention plans for assigned trials.
• Coordinates and conducts patient care visits, including but not limited to: drawing blood, collecting vital signs, performing EKGs, and processing specimens. Assures all procedures are conducted in compliance with the clinical protocol. Processes or ensures proper shipment of lab work.
• Reviews patient journal entries during visitation and documents changes during appointment.
• Interacts with Director/Assistant Director of Site Operations as needed to ensure patient receives appropriate medical evaluation and care when needed.
• Interacts with and maintains close communication with the sponsors Clinical Research Associate.
• Reports serious adverse events and completes reporting to Director/Assistant Director of Site Operations and Principal Investigator.
• Partners with providers to coordinate checkup and documents patient updates post visitation.
• Monitors patient vitals and journal entry trends.
• Attends sponsor Investigator/Study Coordinator meetings as needed for assigned protocols.
• Oversees sponsor database clean-up process. Ensures accurate reporting of trial data to Principal Investigator.
• Trains patients on how to use pump/incline meter and potential side effects of drugs if applicable.
• Upkeeps all regulator documentation including patient binders.
• Issues payment to patients at the end of the visit.
• Other duties as assigned.

Qualifications

Education & Experience Requirements:

Minimum Required:

• Prior experience as a Clinical Research Coordinator or similar role in a medical setting
• CCRC Certification required after qualifying hours met per the ACRP
• At least 2 years of prior experience as a Clinical Research Coordinator or similar role in a medical setting. Experience in Diabetes and/or Endocrine a strong plus
• Prior experience in a patient care role such as MA, LVN, or RN
• CPR/AED Certification
• CCRC Certification a strong plus

This position will require CCRC certification after meeting all Association of Clinical Research Professional (ACRP) CCRC hours.

AAP/EEO Statement

Texas Diabetes & Endocrinology, P.A. (TDE) provides equal employment opportunities (EEO) to all employees and applicants for employment in accordance with applicable federal, state, and local laws. TDE complies with applicable state and local laws governing nondiscrimination in employment in every location in which it has facilities.

Other Duties

Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.

• Pinnacle Clinical Research, LLC
• Come join our team and make a difference as we blaze our way into the future of liver medicine. Pinnacle Clinical Research is dedicated to conducting cutting-edge research with a special focus on fatt...
• Come join our team and make a difference as we blaze the way into the future of liver medicine. Pinnacle Clinical Research is dedicated to conducting cutting-edge research with a special focus on fatt...
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0 Clinical Research Coordinator jobs found in Austin, TX area

• St. David's Medical Center
• Description Introduction St. David's Medical Center is committed to investing in the latest technology enabling nurses t...
• 4/6/2024 12:00:00 AM
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• St. David's North Austin Medical Center
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• Description Introduction Are you looking for a place to deliver excellent care patients deserve? At St. David's Medical ...
• 4/5/2024 12:00:00 AM
• 4/3/2024 12:00:00 AM

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Operations Coordinator - Supply Chain Management - P2P - Remote

• Rochester, MN

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The Procure to Pay Operations Coordinator works collaboratively on multi-disciplinary work groups and projects. Initiates and facilitates activities to establish and enhance financial and operational analyses, supply chain, product management, and other SCM activities and processes. Partners with Mayo departments and the Product Management Committees to review existing supply expenses and to identify supply expense reduction opportunities. Collaborates with staff within Supply Chain Management and customers to implement the identified supply expense reduction opportunities. Provides required support to the Sourcing and Contracting Team including, but not limited to, data collection, input to RFP, vendor analysis, and contract compliance/rebate payment oversight. Conducts research and analysis, benchmarking, and audits to ensure reasonableness and accuracy of information along with identifying and implementing best practices and process improvements for supply chain operations.

This role will close on April 11, 2024 at 11:59 pm.

Bachelor's degree with a minimum of five (5) years' relevant experience in health care, supply chain logistics, finance, business, or nursing; OR, Master's degree with a minimum of two (2) years' relevant experience in health care, supply chain, logistics, finance, business, or nursing required. Certifications may be considered in lieu of experience.  Demonstrated personal computer skills, communication skills, problem solving, continuous improvement and teaming skills. Maintains a broad knowledge of Mayo clinical, financial, and administrative systems/applications and processes. Serves as a resource on department and institutional initiatives; shares knowledge with customers and colleagues. Demonstrated verbal and written communication skills. Assists with SCM continuous improvement initiatives.  Ability to work in a team-oriented environment. Must be adaptable and flexible in an ever-changing work environment. Able to handle/prioritize tasks simultaneously. Basic understanding of accounting principles. Works as a team to provide support to all departments; works with other areas of SCM to ensure exceptional customer service. Ability to manage time to meet required deadlines. Demonstrated knowledge and understanding of Commodity/Service line.  Ability to manage vendor relationships. Comprehension of customer requirements in order to provide solutions to product/service needs. Demonstrated analytical experience. Demonstrated project management skills.

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