Clinical Research Professional (Open Rank)

University of Colorado Anschutz Medical Campus 

Department: Department of Surgery

Job Title: Clinical Research Professional (Open Rank)

Position 0000810346: – Requisition #:38440

Job Summary:

Anschutz Medical Campus is seeking a highly motivated and skilled researcher to work in the Clinical Research Office and the Vascular Surgery Division, in the Department of Surgery. The ideal candidate will have a passion for research and a strong desire to work in a dynamic and collaborative environment. This position provides an opportunity to work on a wide range of complex cases and develop advanced research skills. The Department has state-of-the-art research facilities and a strong culture of interdisciplinary collaboration. The candidate will work closely with renowned experts in the field and have access to mentorship and professional development opportunities. This is a full-time position with a competitive compensation package, including salary and benefits.

Key Responsibilities:

Entry Professional: 

• 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

Intermediate Professional: All of the above and: 

• Independently master study materials, including but not limited to protocols, informed consent forms, and all other essential study documents for assigned studies

• Independently perform study related processes, procedures, and assessments as defined in study protocol and in com