Clinical Research Coordinator II — Gynecologic Trials

CO2000 H. Lee Moffitt Cancer Center and Research Institute, Inc.; United States; On-site; USD 40,000 - 61,000; Full time

Job summary

Moffitt Cancer Center is seeking a Clinical Research Coordinator II to support PI-led trials by enrolling and guiding patients through studies, ensuring safety and protocol adherence.

You'll work with medical staff, regulatory colleagues, and sponsors, handling coordination, data entry, and documentation in line with GCP standards. A developmental path offers growth within the CRC career ladder.

Qualifications

• Bachelor's degree in a scientific, health-related, or business program preferred.
• Two years of clinical trials coordination experience.
• CCRP/CCRC or equivalent preferred.
• Knowledge of GCP and human subjects protections required.
• Proficiency with EMR and trial management systems.

Responsibilities

• Coordinate patient care and enrollment in clinical trials.
• Ensure protocol compliance and monitor subjects on study.
• Liaise between investigators, regulatory staff, and sponsor.
• Maintain accurate documentation per regulatory guidelines.

Skills

Excellent verbal and written comms

Team collaboration

Attention to detail

Strong organizational skills

Education

Bachelor's degree (preferred)

Tools

Microsoft Office Suite

EMR systems

Clinical trial management systems

Data capture/reporting systems

Job description

Moffitt Cancer Center is seeking a Clinical Research Coordinator II to support PI-led trials by enrolling and guiding patients through studies, ensuring safety and protocol adherence.

You'll work with medical staff, regulatory colleagues, and sponsors, handling coordination, data entry, and documentation in line with GCP standards. A developmental path offers growth within the CRC career ladder.