Job Summary

The Hemophilia and Thrombosis Center (HTC) has an opening for a full-time Clinical Research Coordinator. 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. Clinical Science Professionals may also assist with epidemiologic and behavioral studies and/or outcomes research and health services research.

Key Responsibilities

Assist with and oversee the day-to-day operations of clinical trials and studies
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
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
Blood sample collection, processing, and shipping in accordance with IATA regulations.

Work Location

Onsite – this role is expected to work onsite and is located in Aurora, CO.

Job Summary

Key Responsibilities

Assist with and oversee the day-to-day operations of clinical trials and studies
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
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
Blood sample collection, processing, and shipping in accordance with IATA regulations.

Work Location

Onsite – this role is expected to work onsite and is located in Aurora, CO.

Job Summary

Key Responsibilities

Assist with and oversee the day-to-day operations of clinical trials and studies
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
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
Blood sample collection, processing, and shipping in accordance with IATA regulations.

Work Location

Onsite – this role is expected to work onsite and is located in Aurora, CO.

Open Rank Clinical Research Coordinator (Entry – Senior)

University of Colorado Anschutz Medical Campus

13001 E 17th Pl, Aurora, CO 80045, USA