Clinical Research Coordinator, Lymphoma Trials (Hybrid)

Moffitt Cancer Center; Tampa (FL); Hybrid; USD 75,418,000 - 115,017,000; Full time

Job summary

Moffitt Cancer Center is seeking a Clinical Research Coordinator to support patients in therapeutic clinical trials. You will interact directly with patients, screen and enroll participants, educate them on trial processes, and guide them through visits while ensuring safety and protocol compliance.

The role offers a hybrid work model after a 90-day training period, with paid onboarding and access to the CTO Academy.

Qualifications

• Bachelor’s degree in a scientific, health-related, or business administration field is preferred.
• CCRP/CCRC or equivalent certification preferred.
• 1 year of relevant clinical, health-related, scientific, business or research experience preferred.

Responsibilities

• Coordinate patient care with medical staff and document per standards and regulatory guidelines.
• Act as liaison between investigators, regulatory staff, and sponsor.
• Screen, enroll, and monitor study subjects with protocol compliance and safety oversight.
• Maintain data and source documentation and report adverse events.
• Perform administrative duties requiring analysis and judgment within study protocol.
• Work under supervision to implement and coordinate research activities.

Skills

CCRP/CCRC

Clinical research

Regulatory compliance

Education

Bachelor’s degree or higher

Associate degree

1 year relevant experience

Job description

Moffitt Cancer Center is seeking a Clinical Research Coordinator to support patients in therapeutic clinical trials. You will interact directly with patients, screen and enroll participants, educate them on trial processes, and guide them through visits while ensuring safety and protocol compliance.

The role offers a hybrid work model after a 90-day training period, with paid onboarding and access to the CTO Academy.