Full-Time

Clinical Research Coordinator

Clinical Research

Posted on 10/31/2025

University of Oklahoma

University of Oklahoma

No salary listed

Oklahoma, USA

In Person

Category
Biology & Biotech (7)
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Requirements
  • Bachelor's Degree AND 12 months of clinical practice, nursing, or clinical trial or research program coordination experience
  • Equivalency/Substitution: Will accept 48 months of equivalent experience in lieu of a Bachelor's Degree for a total of 60 months experience OR Master's Degree in lieu of experience
  • Oklahoma State licensure is required for Nurses and Physician Assistants. Basic Life Support (BLS)
  • Ability to communicate verbally and in writing
  • Ability to explain the clinical trial study information to the participants
  • Ability to read and follow instructions and guidelines
  • Knowledge of clinical trial protocols
Responsibilities
  • Identifies patients who may be eligible to participate in a clinical trial or research program
  • Performs the initial assessment of potential patients
  • Takes clinical history and completes patient data forms
  • Provides potential patients with study information
  • Obtains informed consent forms
  • Acts as a clinical resource and liaison between physicians, nurses, and laboratory personnel
  • Assists in data management and data analysis
  • Responsible for the initiation, organization, and carrying out of patient follow-up
  • Assesses patient at all follow-up visits
  • Attends various meetings pertaining to the clinical trial or research program
  • May present information
  • May train clinical research staff
  • Performs various duties as needed to successfully fulfill the function of the position
University of Oklahoma

University of Oklahoma

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