Clinical Research Coordinator II: Cancer Trials (Hybrid)

Moffitt Cancer Center; Tampa (FL); Hybrid; USD 32,000 - 49,000; Full time

Job summary

Moffitt Cancer Center in Tampa is seeking a Clinical Research Coordinator II to support investigators in running cancer trials. You will screen, enroll and follow study subjects, educate patients, and help ensure protocol compliance while coordinating with physicians, nurses, and sponsors.

This development role offers a hybrid schedule after a 90-day introductory period, with paid training through the CTO Academy and opportunities to advance as you gain experience in Good Clinical Practices and

Qualifications

• Bachelor's degree with a concentration in a scientific, health related, or business administration program preferred.
• Two (2) years of clinical trials coordination experience.
• Associate's degree considered with two (2) additional years of experience.
• Proficiency in EMR systems, trial management systems, and data capture/reporting systems.

Responsibilities

• Coordinate patient care and enroll/monitor study subjects per protocol.
• Collaborate with medical staff and sponsor for regulatory compliance.
• Manage multiple studies with increasing scope and data capture.

Skills

EMR systems

Clinical trial management systems

Microsoft Office

Database entry

GCP knowledge

Medical terminology

Verbal and written communication

Education

Bachelor's degree in scientific/health/business administration

Tools

CCRP/CCRC

Job description

Moffitt Cancer Center in Tampa is seeking a Clinical Research Coordinator II to support investigators in running cancer trials. You will screen, enroll and follow study subjects, educate patients, and help ensure protocol compliance while coordinating with physicians, nurses, and sponsors.

This development role offers a hybrid schedule after a 90-day introductory period, with paid training through the CTO Academy and opportunities to advance as you gain experience in Good Clinical Practices and