Research Services Clinical Sciences Professional OPEN RANK (Intermediate – Senior)
University of Colorado Anschutz Medical CampusAbout the role
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
Apply for this role
Generate a tailored application kit with a matched cover letter, interview prep, and CV highlights — in under 60 seconds.
Apply Now →Generate Application KitFree account required — sign up in 30s