Oncology Clinical Research Coordinator I

Moffitt Cancer Center

Tampa (FL)

On-site

USD 36,000 - 55,000

Full time

8 days ago

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Job summary

The Clinical Research Coordinator I (CRC I) at Moffitt Cancer Center coordinates clinical research on-site, acting as liaison between investigators, regulatory staff, and sponsors. The CRC I assists with screening, enrollment and follow-up to ensure protocol compliance while documenting data and adverse events.

Under supervision, the CRC I handles diverse administrative tasks, develops competence via structured work assignments, and supports ethical conduct of oncology trials with solid

Qualifications

  • Bachelor's degree preferred in a scientific, health-related or business field.
  • Knowledge of Good Clinical Practices and human subject protection.
  • Experience with EMR and CTMS is a plus but not required.

Responsibilities

  • Coordinate clinical research activities on-site under supervision.
  • Serve as liaison between investigators, regulatory staff and sponsor.
  • Screen, enroll and follow study subjects to ensure protocol compliance.
  • Document data, source documentation and adverse events.
  • Support administrative procedures and maintain study records.

Skills

Verbal communication
Written communication
Interpersonal skills
Microsoft Office
Data entry
Time management
Prioritization
Teamwork

Education

Bachelor's Degree in preferred scientific/health or business administration
Associate degree with 2 years relevant experience

Tools

PowerChart EMR
OnCore CTMS
Clinical trial management systems

Job description

The Clinical Research Coordinator I (CRC I) at Moffitt Cancer Center coordinates clinical research on-site, acting as liaison between investigators, regulatory staff, and sponsors. The CRC I assists with screening, enrollment and follow-up to ensure protocol compliance while documenting data and adverse events.

Under supervision, the CRC I handles diverse administrative tasks, develops competence via structured work assignments, and supports ethical conduct of oncology trials with solid

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