Description
University of Colorado Anschutz Medical Campus
Department: Department of Surgery
Job Title:
Position : – Requisition #:38440
Job Summary:
Anschutz Medical Campus is seeking a highly motivated and skilled researcher to work in the Clinical Research Office and the Vascular Surgery Division, in the Department of Surgery. The ideal candidate will have a passion for research and a strong desire to work in a dynamic and collaborative environment. This position provides an opportunity to work on a wide range of complex cases and develop advanced research skills. The Department has state-of-the-art research facilities and a strong culture of interdisciplinary collaboration. The candidate will work closely with renowned experts in the field and have access to mentorship and professional development opportunities. This is a full-time position with a competitive compensation package, including salary and benefits.
Key Responsibilities:
Entry 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, department, hospital/clinical standard operating procedures and other regulatory guidelines
Participate in subject recruitment efforts, including communicating with patients expressing an interest and all pre-screening/screening activities
Ensure that the necessary supplies and equipment for studies are in stock and in working order
Intermediate Professional: All of the above and:
Independently master study materials, including but not limited to protocols, informed consent forms, and all other essential study documents for assigned studies
Independently perform study related processes, procedures, and assessments as defined in study protocol and in compliance with regulating bodies
Assist Team Leads, Supervisors and/or management with creation and implementation of processes and procedures and quality improvement initiatives
Act as a Primary Coordinator on multiple trials/studies
Assist and train junior team members
Senior Professional: All the above and:
Assist with developing or develops protocol-specific systems and documents including process flows, training manuals, Standard Operating Procedures (SOPs) and Case Report Forms (CRFs). Maintains subject level documentation and prepares documents, equipment and/or supplies
Assist with identifying issues related to operational efficiency and shares results with leadership
Collect information to determine feasibility, recruitment and retention strategies. Employ, evaluate and assist with the implementation of innovative solutions to maximize recruitment and retention
Serve as a resource and participate in study initiation and close out duties
This position will require occasional after-hours and weekend work.
Work Location:
Hybrid – this role is eligible for a hybrid schedule of 4 days per week on campus and as needed for in-person meetings.
Why Join Us
Clinical Research Professional (Open Rank) • Aurora, US
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