Be part of the significant contributions to the prevention and cure of cancer which is based on compassion for our patients, an emphasis on collaboration, and a culture of scientific excellence.

Position Highlights:

• Supports the Principal Investigator (PI) in clinical trials by implementing and coordinating research including administrative procedures at Moffitt Cancer Center.
• As the primary resource for the protocols, the CRC II will coordinate patient care by collaborating with medical staff, and document in accordance with standards and regulatory guidelines.
• Will act as liaison between the investigators, care providers, Moffitt regulatory staff and the sponsor.
• Along with the investigator, the CRC II will screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study.
• The CRC II will perform all Clinical Research Coordinator core support and additional responsibilities of more complex studies, with a higher patient volume.
• The CRC II is responsible for determining methods and procedures for the coordination of newly assigned studies.

 Credentials and Qualifications:

• *Bachelor’s degree with 2 years clinical trials coordination experience
  • *In lieu of a bachelor’s degree, an associate’s degree with 4 years clinical trials coordination experience may be considered
• CCRP/CCRC certification preferred