GI Clinical Research Coordinator: Trials & Data

Moffitt Cancer Center; Tampa (FL); On-site; USD 30,000 - 46,000; Full time

Job summary

Moffitt Cancer Center in Florida seeks a Clinical Research Coordinator Associate to support GI trials. You will assist with data collection, entry, and coordination of non-therapeutic studies, including consent and regulatory documentation, under supervision. This pre-entry role prepares you for progression toward clinical trials careers.

The position emphasizes teamwork, meticulous data handling, and compliance with study protocols, with opportunities to grow within the Clinical Trials Office.

Qualifications

• Associate’s degree required; Bachelor’s degree preferred in scientific, health related or business administration.
• 2 years of relevant experience can substitute the degree with high school diploma or GED.
• Salary range shown as $21.65 - $33.05 per hour; compensation may vary by location and experience.

Responsibilities

• Coordinate data collection and management for assigned clinical trials, typically non-therapeutic.
• Obtain informed consent from study participants and ensure proper documentation.
• Support maintenance of regulatory documents and data entry into study databases.
• Communicate with sponsors and assist with specimen collection as required.

Skills

Clinical trial coordination

Data entry

Informed consent

Regulatory documents

Education

Associate degree

Bachelor's degree preferred

Tools

EDC systems

Job description

Moffitt Cancer Center in Florida seeks a Clinical Research Coordinator Associate to support GI trials. You will assist with data collection, entry, and coordination of non-therapeutic studies, including consent and regulatory documentation, under supervision. This pre-entry role prepares you for progression toward clinical trials careers.

The position emphasizes teamwork, meticulous data handling, and compliance with study protocols, with opportunities to grow within the Clinical Trials Office.