Clinical Research Coordinator II — Hybrid Cancer Trials

Moffitt Cancer Center; Tampa (FL); Hybrid; USD 40,000 - 61,000; Full time

Job summary

Moffitt Cancer Center in Tampa is seeking a dedicated Clinical Research Coordinator (CRC II) to support clinical trials by coordinating patient care and regulatory processes, enrolling and following study subjects, and liaising with investigators and study sponsors.

This role offers a Monday–Friday schedule with a hybrid work arrangement after a 90-day introductory period, and a salary range reflecting clinical trials experience. Career growth and CCRP/CCRC opportunities are available.

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

• Coordinate research including administrative procedures at Moffitt Cancer Center.
• Screen, enroll, and follow study subjects with protocol compliance.
• Serve as liaison between investigators, care providers, and sponsor/regulatory staff.
• Provide core clinical research coordinator support for complex studies with higher patient volume.

Skills

Clinical trials coordination

Regulatory knowledge

Education

Bachelor’s degree

Associate’s degree

CCRP/CCRC certification preferred

Job description

Moffitt Cancer Center in Tampa is seeking a dedicated Clinical Research Coordinator (CRC II) to support clinical trials by coordinating patient care and regulatory processes, enrolling and following study subjects, and liaising with investigators and study sponsors.

This role offers a Monday–Friday schedule with a hybrid work arrangement after a 90-day introductory period, and a salary range reflecting clinical trials experience. Career growth and CCRP/CCRC opportunities are available.