CLINICAL RESEARCH COORDINATOR II - EARLY THERAPEUTICS

Moffitt Cancer Center is hiring a Clinical Research Coordinator II for early therapeutics clinical trials. The role supports investigators by coordinating complex studies, collaborating with medical staff to coordinate patient care, and screening, enrolling, and monitoring study participants while ensuring protocol compliance.

Responsibilities

• 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

Preferred

• CCRP/CCRC certification preferred
• CCRP/CCRC Certification

Benefits

• Monday through Friday schedule
• 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

Company

• Comprehensive cancer hospital and research center
• Tampa, Florida, USA
• http://moffitt.org/
• Founded in 1986
• 10001+ employees

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
• 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

Required skills

• CCRC Certification, CCRP Certification

Preferred skills

• CCRP/CCRC certification preferred

Experience

• 2+ years