Research Services Clinical Sciences Professional, Intermediate to Senior

University of Colorado•Aurora, CO

1d•$49,899 - $66,865•Onsite

About The Position

The University of Colorado Anschutz Medical Campus is seeking a highly motivated and skilled Research Services Professional to join the Clinical Research Office and the Division of Urology within the Department of Surgery. This individual will collaborate closely with Dr. Brian J. Flynn on innovative research focused on Functional and Reconstructive Urology. The ideal candidate will bring a strong passion for clinical research and thrive in a dynamic, team-oriented environment. This role offers the opportunity to contribute to a broad spectrum of complex clinical studies, while gaining advanced research experience in a department known for its state-of-the-art facilities and commitment to interdisciplinary collaboration. The position includes close mentorship from leading experts in the field and access to robust professional development resources. This is a full-time role offering a competitive salary and comprehensive benefits package.

Requirements

Bachelor’s degree in biology, molecular biology, chemistry, genetics or related field
A combination of education and related technical/paraprofessional experience may be substituted for the bachelor’s degree on a year for year basis.
Applicants must meet minimum qualifications at the time of hire.
Knowledge and understanding of federal regulations and Good Clinical Practice (GCP)
Ability to communicate effectively, both in writing and orally
Ability to establish and maintain effective working relationships with employees at all levels throughout the institution
Outstanding customer service skills
Demonstrated commitment and leadership ability to advance diversity and inclusion
Knowledge of basic human anatomy, physiology medical terminology
Ability to interpret and master complex research protocol information
Applicants must be legally authorized to work in the United States without requiring sponsorship. We are unable to provide work visa sponsorship and employment authorization for this position now or in the future.

Nice To Haves

Bachelor’s degree in science or health related field
Experience with electronic data capture systems (e.g. EMR or EHR and data management systems)

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 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