Clinical Sciences Professional (Open Rank: Intermediate – Senior)
University of ColoradoAbout the role
Description
University of Colorado Anschutz Medical Campus
Department: Ophthalmology
Job Title: Clinical Sciences Professional (Open Rank: Intermediate – Senior)
Position #00841243 – Requisition #: 38061
Job Summary:
The Department of Ophthalmology has an opening for 1.0 FTE clinical intermediate – senior professional to support our Cornea division. The successful candidate will coordinate clinical studies, assists with adherence to IRB/regulatory requirements, enroll and correspond with study participants, act as liaison to industry sponsors of research studies, clinical research organizations, the Federal Drug Administration, and other participating centers, maintain study databases and files, create and monitor study budgets and generate and process invoices. Provide ophthalmic assistance to the Cornea division faculty, fellow and rotating resident, providing ancillary screening and testing as necessary.
Key Responsibilities:
Intermediate 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, departme
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