Clinical Research Coordinator Float-Clinical Trials Management Office

About the role

The Clinical Research Coordinator- Float is responsible for coordinating and performing daily clinical research activities in various departments and divisions within the College of Medicine (COM) Center for Clinical Research Management (CCRM).

Responsibilities

• Assess patient records to identify patients eligible for specified clinical research protocols.
• Recruit, interview, and enroll patients.
• Administer informed consent and ensure compliance with regulatory and sponsor requirements.
• Coordinate scheduling and follow-through of patient care appointments, procedures, and diagnostic testing.
• Collect, process, and evaluate biological samples.
• Administer, evaluate, and calculate standardized scoring of diagnostic, psychological, or behavioral tests or questionnaires.
• Monitor patients for adverse reactions and notify appropriate clinical professionals.
• Document unfavorable responses and report to research sponsors and regulatory agencies.
• Evaluate patients for compliance with study protocols.
• Collect, extract, code, and analyze clinical research data.
• Generate reports and ensure the validity of collected data.
• Support activities to ensure compliance with Institutional Review Boards (IRB), FDA, federal, state, and industry sponsor regulations.
• Coordinate and prepare for external quality assurance and control reviews by IRB, federal, or industry sponsors.
• Contribute to the development of new research protocols and establish study goals.

Requirements

• Minimum Education: Bachelor’s Degree in biological sciences, health sciences, social sciences, or other medical field.
• Minimum Experience: One year experience in a clinical research capacity.
• Computer experience required.
• Experience or knowledge in coordinating clinical trials preferred.
• Knowledge of medical terminology desired.
• Clinical research certification from an accredited certifying agency desired.
• Experience using Microsoft applications desired.
• Knowledge of data base systems such as RedCap, Medidata, Rave, etc. desired.

Qualifications

• Successful completion of a background check.
• Ability to pass a pre-employment physical, including a drug screen.

Benefits

Qualified candidates may be requested to complete a pre-employment physical, including a drug screen. Final candidates are subject to a background check. A drug screen or physical may be required during the post-offer process.

Pay

Details about pay are not specified in this posting.

Schedule

Details about schedule are not specified in this posting.