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Clinical Sciences Professional (Entry – Intermediate Level)

University of Colorado
UKRemotefull_timeVerifiedPosted 29 Jul 2025
💰 $67,061/yr($48,446/yr$67,061/yr)

About the role

Clinical Sciences Professional (Entry – Intermediate Level) - 37394 University Staff 

Description

 

University of Colorado Anschutz Medical Campus

School of Medicine | Department of Medicine | Division of Gastroenterology & Hepatology

Job Title: Clinical Sciences Professional (Entry – Intermediate Level)

Position: #00837797 – Requisition: #37394

Job Summary:

This Research Services Clinical Sciences Professional will help support the IBD (inflammatory bowel diseases) division section of Gastroenterology.

This position will be a part of a team that includes supportive research personnel (regulatory, budget, coordinators) and medical personnel all led by the principal investigator and the GI division research leadership. The Clinical Sciences Professional will participate in clinical research projects including studies examining pancreatitis and therapeutic endoscopy. The position requires an ability to work independently, but collaboratively, have attention to detail, and be able to maintain organized protocol documentation and data. The studies we conduct require in-person and telephone interactions with participants/patients/staff; thus, we are seeking a candidate who is a “people person” and can interact well with others. 

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

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Company

University of Colorado

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