Open Rank Clinical Research Coordinator (Entry – Senior)

University of Colorado•Aurora, CO

1d•Onsite

About The Position

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.

Requirements

Bachelor’s degree in any field
One (1) year clinical research or related experience (for Intermediate Level)
Two (2) years clinical research or related experience (for Senior Level)
A combination of education and related technical/military/paraprofessional experience may be substituted for a bachelor’s degree on a year for year basis
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
Knowledge of basic human anatomy, physiology, and medical terminology
Ability to interpret and master complex research protocol information
Proficient in Microsoft Office
Conscientious and meticulous in data extraction and data entry
Ability to work well in a team environment, but also able to work independently
Ability to adhere to local and federal regulations and ethical codes with respect to the protection of human subjects and patient confidentiality and privacy
Ability to resolve conflicts in a constructive manner
Ability to understand, learn, and adhere to department Standard Operating Procedures
Ability to adjust to and meet new or unanticipated work challenges
Proficient in study-specific procedures and techniques; updating, learning, and implementing changes when industry, University, or Section standards change

Nice To Haves

Bachelor’s degree in science or health related field
Three (3) years of clinical research or related experience
Experience with electronic data capture systems (e.g. EMR or EHR and data management systems)
Experience with and proficient in adult and pediatric phlebotomy

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.