- 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.
- 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.
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Clinical Research Coordinator - Norman, United States - The University of Oklahoma
Description
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.Duties:
Required Education:
Bachelor's Degree AND:
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.
Skills:
Certifications:
Advertised Physical Requirements:
Departmental Preferences:
RN
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