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Research Services Clinical Sciences Professional OPEN RANK (Intermediate – Senior)

University of Colorado Anschutz Medical Campus
United Statesfull_timeVerifiedPosted 26 Jun 2026
💰 $78,665/yr($54,302/yr$78,665/yr)

About the role

Research Services Clinical Sciences Professional OPEN RANK (Intermediate – Senior)(

Job Number:

 40318)

Description

 

University of Colorado Anschutz Medical Campus

Department: SOM - Orthopedics

Job Title: Research Services Clinical Sciences Professional OPEN RANK (Intermediate – Senior)

Position #: 00837810 – Requisition #:40318

 

Job Summary:

This position will act as a clinical research coordinator for the Emily Lindley Research Lab, assisting with studies related to non-opioid alternatives for treatment of chronic musculoskeletal pain. This position is posted as “open rank,” meaning the selected candidate may be hired at either the intermediate or senior level, depending on the relevant experience of the selected candidate, as well as the business needs and budgetary considerations of the hiring department.

 

Intermediate 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.

 

Senior 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. Senior Clinical Science Professionals may also assist with epidemiologic and behavioral studies and/or outcomes research and health services research. Some Assignments will not move beyond this level.

 

Key Responsibilities:

All Levels:

  • 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

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Company

University of Colorado Anschutz Medical Campus

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