Clinical Research RN I — Cancer Trials Coordinator

Moffitt; Florida; On-site; USD 51,000 - 78,000; Full time

Job summary

Moffitt Southshore is seeking a Clinical Research RN I to coordinate opening new protocols, evaluate patients, and enroll eligible participants in cancer trials. The CRN I delivers direct patient care, educates patients, and documents according to GCP and regulatory standards.

The role collaborates with investigators, regulatory staff, and sponsors to ensure protocol compliance and proper data capture. Onsite position with competitive pay.

Qualifications

• BSN from ACEN/CCNE accredited institution with Florida RN license and 1 year nursing experience.
• ADN/ASN with Florida RN license and 3 years nursing experience.
• NPDB self-query prior to employment; no NPDB reports unless appealed.

Responsibilities

• Coordinate opening of new protocols and patient evaluation for trials.
• Register eligible patients and coordinate protocol-related care.
• Provide direct patient care and education per protocol needs.
• Maintain regulatory files and document adverse events.
• Monitor subject accruals and protocol tracking with the team.

Skills

RN license

Clinical research

Good Clinical Practice

Patient education

Education

BSN with Florida RN license or ADN/ASN with Florida RN license

Job description

Moffitt Southshore is seeking a Clinical Research RN I to coordinate opening new protocols, evaluate patients, and enroll eligible participants in cancer trials. The CRN I delivers direct patient care, educates patients, and documents according to GCP and regulatory standards.

The role collaborates with investigators, regulatory staff, and sponsors to ensure protocol compliance and proper data capture. Onsite position with competitive pay.