Overview
Responsible for the coordination and conduct of clinical trials, under the direction of the Principal Investigator and the Manager/Director, in accordance with the standards of good clinical practice and FDA regulations.
Responsibilities
- Coordinate and conduct clinical trials in alignment with GCP and FDA requirements under supervision of the Principal Investigator and Manager/Director.
Required Qualifications
- Graduate of an accredited school of nursing or a diploma program. For new hires after 2012, Bachelor of Science Degree in nursing (BSN) is required within the specified timeframe as outlined in the New Hire BSN Agreement policy (126.045).
- Certification as a Clinical Research Coordinator within one (1) year of eligibility.
- Appropriate training in Human Subject Protection and Safe Shipping/Handling of Bio-Hazardous Specimens (completed within thirty (30) days of hire).
- Valid driver's license and the ability to drive to off-site locations.
Preferred Qualifications
- Knowledge of commonly used computer applications.
- Experience in a clinical research and/or a medical/surgical or critical care setting.
- Ability to initiate work without supervision.
- Demonstrated proficiency in interpersonal skills with staff, subjects, families, physicians, and sponsor/auditors of clinical trials.
Licenses and Certifications
- BLS: Basic Life Support/CPR
- FL RN: Florida Registered Nurse License
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