Clinical Research Coordinator II — Cancer Trials Lead

Moffitt Cancer Center; Ruskin (FL); Hybrid; USD 55,000 - 75,000; Full time

Job summary

The Clinical Research Coordinator II (CRC II) at Moffitt Cancer Center is a mid-level position in the CRC career path within Clinical Trials. The CRC II supports the PI in coordinating research including administrative procedures, and may assist PI-sponsored IND/IDE trials.

It serves as the primary resource for protocols, coordinating patient care with medical staff and documenting in line with standards and regulatory guidelines.

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.

Responsibilities

• Assist PI in conducting clinical trials by implementing and coordinating research activities.
• Screen, enroll, and follow study subjects while ensuring protocol compliance and regulatory standards.
• Coordinate patient care by collaborating with medical staff and documenting in accordance with guidelines.
• Serve as liaison between investigators, care providers, regulatory staff, and sponsors.
• Provide core CRC support and handle more complex studies with increasing patient volume.

Skills

Clinical trials coordination

Education

Bachelor’s degree with 2 years clinical trials coordination experience

Associate’s degree with 4 years clinical trials coordination experience

Job description

The Clinical Research Coordinator II (CRC II) at Moffitt Cancer Center is a mid-level position in the CRC career path within Clinical Trials. The CRC II supports the PI in coordinating research including administrative procedures, and may assist PI-sponsored IND/IDE trials.

It serves as the primary resource for protocols, coordinating patient care with medical staff and documenting in line with standards and regulatory guidelines.