Hybrid Clinical Research Coordinator I — Cancer Trials

Moffitt Cancer Center; Land O' Lakes (FL); Hybrid; USD 55,000 - 75,000; Full time

Benefits offered by this job

Relocation assistance

Job summary

Moffitt Cancer Center is seeking a Clinical Research Coordinator to enroll and educate patients in therapeutic trials, ensuring smooth trial progress and patient safety. You will collaborate with physicians, nurses, and sponsors while navigating regulatory requirements.

After a 90‑day training period, the role offers a hybrid schedule mixing remote and on-site work. Relocation assistance may be provided, with opportunities for career development through CTO Academy.

Qualifications

• Bachelor’s degree preferred in scientific, health-related, or business administration fields.
• In lieu of bachelor’s degree, an associate’s degree with 2 years of relevant experience is acceptable.
• CRCP/CCRC or equivalent certification is preferred.

Responsibilities

• Coordinate patient care by collaborating with medical staff and document in accordance with standards and regulations.
• Act as liaison between investigators, regulatory staff, and sponsor.
• Screen, enroll, and follow study subjects with protocol compliance and adverse event monitoring.
• Manage data and source documentation and adverse event reporting.
• Support administrative procedures and coordinate research activities under supervision.

Education

Bachelor’s degree (preferred)

Associate’s degree with 2 years relevant experience

CCRP/CCRC or equivalent preferred

Job description

Moffitt Cancer Center is seeking a Clinical Research Coordinator to enroll and educate patients in therapeutic trials, ensuring smooth trial progress and patient safety. You will collaborate with physicians, nurses, and sponsors while navigating regulatory requirements.

After a 90‑day training period, the role offers a hybrid schedule mixing remote and on-site work. Relocation assistance may be provided, with opportunities for career development through CTO Academy.