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Part-time Research Services Clinical Sciences Professional (Open Rank, Entry or Intermediate) (0.5 FTE – 20 hours/week)

University of Colorado
United Statespart_timeVerifiedPosted 18 Nov 2025
💰 $33,530/yr($24,223/yr$33,530/yr)

About the role

Part-time Research Services Clinical Sciences Professional (Open Rank, Entry or Intermediate) (0.5 FTE – 20 hours/week) - 38296 University Staff 

Description

 

University of Colorado Anschutz Medical Campus

Department: Medicine – Division of Renal Diseases and Hypertension

Job Title: Part-time Research Services Clinical Sciences Professional (Open Rank, Entry or Intermediate) (0.5 FTE – 20 hours/week)

Position #:00842162 – Requisition #:38296

Job Summary:

Clinical Science Professionals perform clinical research related functions which may include patient-oriented research or research conducted with human subjects. Patient-oriented research includes mechanisms of human disease, therapeutic interventions, clinical trials, or development of new technologies. Clinical Science Professionals may also assist with epidemiologic and behavioral studies and/or outcomes research and health services research. This position will work with study physicians and staff both locally and nationally as a part of local studies and a multi-center studies and will be responsible for study coordination, participant recruiting, consent, and scheduling, performing study visits, processing of research blood samples and other study samples, institutional review board requirements, tracking of study costs, assisting with imaging procedures, entering data and other study-related duties.

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

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Company

University of Colorado

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