Entry-Level Clinical Research Coordinator (Oncology)

Moffitt Cancer Center; Tampa (FL); On-site; USD 74,390,000 - 115,030,000; Full time

Job summary

The Clinical Research Coordinator I (CRC I) at Moffitt Cancer Center coordinates clinical research activity on-site, serving as the primary resource for study protocols and liaison between investigators, regulatory staff, and sponsors.

Under supervision, the CRC I screens, enrolls, and follows subjects, ensures protocol compliance, and handles data, source documentation, and adverse event reporting; performs duties with mentorship and structured guidance.

Qualifications

• Bachelor-level education in science, health, or business administration is preferred.
• If no Bachelor's, an Associate's degree plus two years of relevant experience is allowed.

Responsibilities

• Coordinate on-site clinical research activities under supervision.
• Screen, enroll, and follow study subjects per protocol.
• Ensure data capture and adverse event reporting with regulatory compliance.
• Provide administrative support and liaise with investigators, regulatory staff and sponsor.

Skills

Clinical research

Communication skills

Documentation

Regulatory knowledge

EMR knowledge

Education

Bachelor's Degree in scientific/health related or business administration

Associate's degree with 1 year additional relevant experience

Tools

PowerChart EMR

OnCore

Job description

The Clinical Research Coordinator I (CRC I) at Moffitt Cancer Center coordinates clinical research activity on-site, serving as the primary resource for study protocols and liaison between investigators, regulatory staff, and sponsors.

Under supervision, the CRC I screens, enrolls, and follows subjects, ensures protocol compliance, and handles data, source documentation, and adverse event reporting; performs duties with mentorship and structured guidance.