Clinical Research Coordinator

University of Colorado•Aurora, CO

6d•Onsite

About The Position

The Division of Pulmonary, Allergy, and Critical Care Medicine at the University of Colorado Anschutz Medical Campus is seeking an organized individual for a full-time Clinical Research Coordinator position. This role will support the Asthma Research Program with both industry and grant-funded clinical protocols. The coordinator will be responsible for screening, enrollment, study visits, data management, regulatory compliance, and other duties associated with performing clinical research activities. Excellent organizational, time management, and communication skills are essential. The successful candidate will be a productive member of the research team, capable of working independently and as part of a team, and able to support multiple ongoing clinical studies simultaneously. Flexible work hours, including infrequent evenings or weekends, may be required. This position involves close collaboration with Principal Investigators, other research coordinators, and laboratory members in a cooperative environment with growth potential.

Requirements

Bachelor of Science in Nursing (BSN) degree. An Associate Degree in Nursing (ADN) degree and two (2) additional years of experience will substitute for the BSN degree.
Three (3) years of clinical research or related experience.
Current licensure as a registered nurse.
Applicants must meet minimum qualifications at the time of hire.
Applicants must be legally authorized to work in the United States without requiring sponsorship.
Advanced 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.

Nice To Haves

Four (4) years of clinical research or related experience.
Experience with electronic data capture systems (e.g., EMR or EHR and data management systems).

Responsibilities

Perform clinical visits for asthma studies, including lung function testing, spirometry, methacholine, and blood draws.
Take part in recruitment and managing aspects of clinical studies.
Follow up with participants throughout study progression.
Follow research protocols and manual of procedures.
Participate in the regulatory management of study protocols.