Clinical Research Coordinator

CLINICAL RESEARCH COORDINATOR I – Moffitt Cancer Center

Are you looking for an opportunity to impact lives and be a central part of a team in the fight against cancer? As a Moffitt Clinical Research Coordinator you’ll bring hope to patients by delivering tomorrow’s cancer treatments today. You will interact directly with patients, enrolling, educating and guiding them through clinical trials, ensuring safe and smooth progress.

• Coordinate patient care by collaborating with medical staff and documenting in accordance with standards and regulatory guidelines under the direction of a mentor or supervisor.
• Act as liaison between investigators, Moffitt regulatory staff, and the sponsor.
• Assist in screening, enrolling, and following study subjects, ensuring protocol compliance and close monitoring.
• Responsible for data and source documentation and adverse event reporting.
• Perform diverse administrative duties requiring sound judgment and a high level of knowledge of study protocol.
• Work under general supervision and direction from the supervisor and Principal Investigator to implement and coordinate research, including administrative procedures.

• Bachelor’s degree (preferred field of study: scientific, health related, or business administration) with one (1) year of relevant clinical, health related, scientific, business or research experience.
• In lieu of a bachelor’s degree: associate’s degree with two (2) years of relevant experience.
• CCRP/CCRC or equivalent preferred.

• Seniority level:
  Entry level
• Employment type:
  
  Full-time
• Job function:
  Research, Analyst and Information Technology
• Industries:
  Hospitals and Health Care