Open Rank Clinical Services Coordinator (Entry – Senior)

University of Colorado

1d•Hybrid

About The Position

The Interstitial Lung Disease (ILD) Program at the University of Colorado, School of Medicine is hiring two (2) full-time (1.0 FTE) Clinical Research Coordinators for an active clinical research program. This position will be supervised by the lead CRC in the ILD program under the direction of the Director of ILD. This position will primarily focus on the recruitment and retention of subjects in investigator-initiated studies and clinical trials.

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.
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.
Knowledge of basic human anatomy, physiology, and medical terminology.
Ability to interpret and master complex research protocol information.
Strong organizational skills with the ability to prioritize workload, adapt to changing demands, and work independently in a high-volume environment.
Ability to apply critical thinking to identify issues, develop solutions, and adapt to changing circumstances.
Proven ability to maintain accuracy and consistency while managing complex or high-volume tasks.

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).

Responsibilities

Serve as the primary clinical research coordinator for investigator-initiated and clinical research protocols.
Collaborates with investigators, clinical staff, and research staff to ensure study procedures are performed per protocol and properly documented.
Ensure protocol specific compliance and compliance with FDA, OHRP, GCP, IRB, HIPAA, UCD, and affiliates.
Independently master study materials, including but not limited to protocols, informed consent forms, and all other essential study documents for assigned studies.
Independently perform study related processes, procedures, and assessments as defined in study protocol and in compliance with regulating bodies.
May be called upon to perform phlebotomy, EKG, spirometry, and vital measurements including blood pressure.