Clinical Research Coordinator I - Heme/Myeloid (Hybrid)

Moffitt Cancer Center; Tampa (FL); Hybrid; USD 52,000 - 65,000; Full time

Benefits offered by this job

Hybrid work after training period

Relocation assistance

Paid training and orientation

CTO Academy

Job summary

Moffitt Cancer Center in Tampa, FL is seeking a Clinical Research Coordinator I to support Heme/Myeloid trials. This role involves direct patient interaction, screening and enrolling participants, educating them about trial participation, and guiding them through study procedures within a therapeutic clinical trial framework.

You will work with physicians, pharmacists, nurses, and data managers to ensure protocol compliance, data integrity, and safety reporting, while benefiting from a hybrid

Qualifications

• Coordinate patient care and ensure protocol adherence under supervisor.
• Screen, enroll, and follow study subjects with regulatory compliance.
• Maintain data integrity and adverse event reporting.
• Prepare documentation and communicate with sponsors and team.

Responsibilities

• Coordinate patient care by collaborating with medical staff and document in accordance with guidelines.
• Screen, enroll, and monitor subjects while ensuring protocol compliance.
• Manage data and source documentation and adverse event reporting.
• Support trial logistics and administrative procedures under supervision.

Skills

Clinical coordination

Regulatory knowledge

Documentation

Customer service

Education

Bachelor’s degree (preferred in scientific/ health related/ business)

Associate’s degree with 2 years relevant experience

Tools

CCRP/CCRC certification preferred

Job description

Moffitt Cancer Center in Tampa, FL is seeking a Clinical Research Coordinator I to support Heme/Myeloid trials. This role involves direct patient interaction, screening and enrolling participants, educating them about trial participation, and guiding them through study procedures within a therapeutic clinical trial framework.

You will work with physicians, pharmacists, nurses, and data managers to ensure protocol compliance, data integrity, and safety reporting, while benefiting from a hybrid