Sr. Clinical Research Coordinator

Position Introduction:

Coordinates a clinical research program by identifying and assessing patients, distributing information, acting as a clinical resource, managing data, conducting follow-up care for patients, attending meetings on the program, and supervising program personnel.  Identifies patients who may be eligible to participate in the research program. Performs the initial assessment of potential patients. Obtains clinical history and completes patient data forms. Provides potential patients with study information. Obtains informed consent forms. Acts as the immediate clinical resource and the liaison between physicians, nurses, laboratory personnel, etc. Performs data management and data analysis. Responsible for the initiation, organization, and carrying out of patient follow-up. Assesses patients at all follow-up visits.  Attends various meetings pertaining to the research program May present information. May assume the lead role when the supervisor is not available to ensure adherence to protocol. May lead and train research personnel. Performs various duties as needed to fulfill the function of the position successfully.

View full job descripton

Required Education and Experience:

• Bachelor's degree in a health profession, physical science, biological science, or nursing.
• 48 months of clinical practice, nursing, or research program coordination experience.

Equivalency/Substitution: Will accept 48 months clinical practice or research program coordinator experience in lieu of the Bachelor's Degree for a total of 96 months experience.

Required Certifications and Licenses:

One of the following licensures is required, based on the assigned area or department:

• Registered Nurse (RN) licensure through the Oklahoma Board of Nursing; or
• Physician Assistant (PA) licensure through the Oklahoma Medical Board