Clinical Research Coordinator
University of Oklahoma
- Oklahoma
- Permanent
- Full-time
- Identifies and assesses patients who may be eligible to participate in a clinical trial or research program, distributes information, acts as a clinical resource, manages data, conducts follow-up care for patients, and attends meetings pertaining to the program.
- 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.
- May perform a physical exam during the assessment.
- 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.
- 12 months of clinical practice, nursing, or clinical trial or research program coordination experience.
- Knowledge of clinical trial protocols.
- 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.
- Oklahoma State licensure is required for Nurses and Physician Assistants. Basic Life Support (BLS)
- Physical: Sitting for prolonged periods. Manual dexterity. Speaking and listening. Reaching, bending, standing and stooping.
- Environmental: Clinic Environment. Exposure to infectious diseases.