Note: The job is a remote job and is open to candidates in USA. Moffitt Cancer Center is a National Cancer Institute-designated Comprehensive Cancer Center dedicated to the prevention and cure of cancer. The Clinical Research Coordinator I coordinates patient care and clinical trial activities, including screening and enrolling study subjects, maintaining documentation, monitoring protocol compliance, and collaborating with investigators, sponsors, and clinical research teams.
Responsibilities
- Coordinate patient care by collaborating with medical staff and document in accordance with standards and regulatory guidelines with direction of a mentor or supervisor
- Act as liaison between the investigators, Moffitt regulatory staff and the sponsor
- Will assist to screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study
- Responsible for data and source documentation and adverse experience reporting
- Perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study protocol
- Will work under general supervision and direction from the supervisor and Principal Investigator to implement and coordinate research, including administrative procedures
Skills
- Bachelor's degree (preferred field of study scientific, health related or business administration program) with one (1) year of relevant clinical, health related, scientific, business or research experience
- In lieu of bachelor's degree, Associate's degree with 2 years of relevant clinical, health related, scientific, business or research experience
- CCRP/CCRC or equivalent preferred
Benefits
- Monday through Friday schedule and hybrid work (mix of remote and on-site) after passing a 90-day introductory and training period.
- Paid training and orientation through its CTO (Clinical Trails Office) Academy.
- Relocation assistance may be provided.
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