Senior Clinical Research Coordinator – Trials & Data

CO2000 H. Lee Moffitt Cancer Center and Research Institute, Inc.; United States; On-site; USD 44,000 - 67,000; Full time

Job summary

Moffitt Cancer Center seeks a Clinical Research Coordinator III to support the Lymphoma Data Management program. The role coordinates clinical research activities, collaborates with medical staff, and ensures protocol compliance and regulatory adherence in a fast-paced cancer research environment.

The CRC III acts as a subject matter expert, guiding lower-level coordinators, managing diverse workloads, and maintaining high-quality data capture across EMR and trial management systems.

Qualifications

• Bachelor’s degree with 4 years of experience in clinical trials coordination.
• In lieu of a bachelor’s degree, Associate’s degree with 6 years clinical trials coordination experience may be considered.
• CCRP/CCRC certification required.

Responsibilities

• Coordinate patient care with medical staff and document per standards and regulatory guidelines.
• Serve as liaison between investigators, care providers, regulatory staff and sponsor.
• Screen, enroll, and follow study subjects to ensure protocol compliance and monitoring.
• Carry out CRC core support and higher workload responsibilities.
• Work independently with moderate oversight to implement and coordinate research.

Skills

Communication skills

EMR systems

Trial management systems

Education

Bachelor's degree

Associate's degree

CCRP/CCRC certification

Tools

EMR systems

Clinical trial management systems

Job description

Moffitt Cancer Center seeks a Clinical Research Coordinator III to support the Lymphoma Data Management program. The role coordinates clinical research activities, collaborates with medical staff, and ensures protocol compliance and regulatory adherence in a fast-paced cancer research environment.

The CRC III acts as a subject matter expert, guiding lower-level coordinators, managing diverse workloads, and maintaining high-quality data capture across EMR and trial management systems.