Research Services Clinical Sciences Professional, Intermediate to Senior

University of Colorado Anschutz

Department: Surgery

Job Title: Clinical Research Services Entry Professional- Functional and Reconstructive Urology (FRU)

Position #:00834499 – Requisition #:40509

Job Summary:

The University of Colorado Anschutz Medical Campus is seeking a highly motivated and skilled Research Services Professional to join the Clinical Research Office and the Division of Urology within the Department of Surgery. This individual will collaborate closely with Dr. Brian J. Flynn on innovative research focused on Functional and Reconstructive Urology. The ideal candidate will bring a strong passion for clinical research and thrive in a dynamic, team-oriented environment. This role offers the opportunity to contribute to a broad spectrum of complex clinical studies, while gaining advanced research experience in a department known for its state-of-the-art facilities and commitment to interdisciplinary collaboration. The position includes close mentorship from leading experts in the field and access to robust professional development resources. This is a full-time role offering a competitive salary and comprehensive benefits package.

Key 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

• Interview prospective subjects for a variety of research clinical trials. Educate potential subjects on the details of the studies through phone contacts and personal interviews

• Schedule subject participation in research clinical trial, coordinating availability of necessary space, and clinical research support (e.g., physician, nurse practitioner, laboratory, radiology, pharmacy)

• Collect, code, and analyze data obtained from research in an accurate and timely manner

• Adhere to research regulatory standards

• Maintain detailed records of studies to ensure compliance with requirements of the Food and Drug Administration (FDA), study protocols, department, hospital/clinical standard operating procedures and other regulatory guidelines

• Participate in subject recruitment efforts, including communicating with patients expressing an interest and all pre-screening/screening activities

• Ensure that the necessary supplies and equipment for studies are in stock and in working order

This position will require occasional after-hours and weekend work.

This description is a summary only and describes the general level of work being performed, it is not intended to be all-inclusive. The duties of this position may change from time to time and/or based on business need. We reserve the right to add or delete duties and responsibilities at the discretion of the supervisor and/or hiring authority.

Work Location: