Sr. Clinical Research Coordinator
About The Position
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.
Requirements
- Bachelor's degree in a health profession, physical science, biological science, or nursing.
- 48 months of clinical practice, nursing, or research program coordination experience.
- Registered Nurse (RN) licensure through the Oklahoma Board of Nursing; or Physician Assistant (PA) licensure through the Oklahoma Medical Board
Nice To Haves
- 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.
Responsibilities
- Identifying and assessing patients
- Distributing information
- Acting as a clinical resource
- Managing data
- Conducting follow-up care for patients
- Attending meetings on the program
- Supervising program personnel
- Performing the initial assessment of potential patients
- Obtaining clinical history and completing patient data forms
- Providing potential patients with study information
- Obtaining informed consent forms
- Acting as the immediate clinical resource and the liaison between physicians, nurses, laboratory personnel, etc.
- Performing data management and data analysis
- Responsible for the initiation, organization, and carrying out of patient follow-up
- Assessing patients at all follow-up visits
- Attending various meetings pertaining to the research program
- Presenting information
- Assuming the lead role when the supervisor is not available to ensure adherence to protocol
- Leading and training research personnel
- Performing various duties as needed to fulfill the function of the position successfully
Benefits
- Benefits Eligible: Yes
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What This Job Offers
Job Type
Full-time
Career Level
Senior
