Clinical Trials Coordinator

Colorado State University•Fort Collins, CO

1d•$50,000 - $60,000•Onsite

About The Position

The Department of Clinical Sciences mission is to assure the health and productivity of animals to meet societal needs through high quality educational programs for professional veterinary medical students, graduate veterinarians, and the public through a faculty and veterinary medical center of excellence, and to advance and disseminate comparative biomedical knowledge in an environment of interdisciplinary collaboration. The Flint Animal Cancer Center at Colorado State University is seeking applications to fill the position of Clinical Trials Coordinator. This position will manage protocol compliance for all enrolled clinical trials patients, assist in patient recruitment, provide assistance to the Clinical Trials Technician such as patient receiving, collecting samples and data entry, and perform various study-related administrative tasks such as shipping lab supply ordering and updating clinical trials patient rosters. This person is also responsible for maintaining study binders for all patients enrolled into clinical trials and ensuring that they are complete, as well as entering information into online data capture systems for clinical trials. This position is fully in-person.

Requirements

BS degree in Biology or closely related field.
Associate degree with 2 years of related experience.
More than three years of experience as a veterinary technician or in human clinical trials.
Previous experience working in a laboratory setting processing samples such as plasma, serum, peripheral blood mononuclear cells, etc.
Ability to work with others in a team environment.
Must be legally authorized to work in the United States by the proposed start date. The department will not provide visa sponsorship for this position.

Nice To Haves

Demonstrated interest in clinical trials-related research, and excellent organization skills and attention to detail.
Previous experience in clinical trials.

Responsibilities

Ensure protocol compliance for all patients enrolled in clinical trials including internal monitoring of clinical trial data for quality and accuracy, sample collection/processing/shipment, and maintenance of patient study records.
Must maintain a working knowledge of protocols of all clinical trials that are open for enrollment.
Completion of other administrative tasks as needed such as study drug inventory, study budget tracking, scheduling appointments for trials patients, updating the clinical trials patient enrollment roster, assembling patient binders, communications with Principal Investigators at CSU and other collaborating study sites, etc.
Assist in clinical trial participant enrollment, including assessment of eligibility criteria and obtaining owner informed consent.
Provide assistance to clinical trials technicians as needed.