Senior Clinical Research Coordinator

3 weeks ago


Aurora, United States University of Colorado Full time
Senior Clinical Research Coordinator-33284University Staff

Description

University of Colorado Anschutz Medical Campus

Department: Orthopedics

Job Title: Clinical Sciences Senior Professional

Position #00808929 – Requisition #33284

Job Summary:

The Dragoo Research Program, located at the Inverness Orthopedics and Spine Center - Steadman Hawkins Clinic, is seeking a Senior Clinical Research Coordinator (Sr. CRC) with clinical research experience. The Sr. CRC role requires proficient communication with several entities, physicians, and researchers, as well as leading clinical trials and regulatory requirements for human subject research. 

The Sr. CRC will be responsible for maintaining a thorough understanding of assigned human subject research protocols and projects, particularly focusing on the biobanking initiative (CUREBANK), investigator-initiated studies, and industry-sponsored research. The Sr. CRC will report to the Program Manager and provide technical and administrative assistance to Dr. Jason Dragoo’s research team. Duties include engagement in technical research activities, laboratory functions, data entry and oversight using electronic systems, and ensuring compliance with reporting requirements for protocols and projects.

Responsibilities:

Assist with and oversee the day-to-day operations of clinical trials and studies Obtain study subject’s medical history and current medication information, reviews research protocol inclusion/exclusion criteria, and confirms eligibility of subject to participate in clinical trial Perform informed consent process or ensures that the informed consent process has occurred, is properly documented, and that informed consent form documents are filed as required Updates study calendar of various clinical protocols and coordinates logistics needed for successful completion of the studies. Serve as a primary contact for regulatory bodies, study participants, Sponsors, and fellow researchers, handling tasks such as scheduling, confirming appointments, etc. Screens, recruits, and obtains informed consent from potential candidates for research studies. Coordinates study clinic visits, and performs protocol-specific research activities including, but not limited to, concomitant medicine checks, physical histories, AE/SAE/UAP checks.

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