Clinical Research Coordinator I - Breast

Summary

Moffitt Cancer Center is a cancer research and treatment center focused on the prevention and cure of cancer. The Clinical Research Coordinator I will support breast cancer clinical trials by coordinating patient care, screening and enrolling study subjects, ensuring protocol compliance, managing research data and documentation, and collaborating with investigators, sponsors, and clinical teams.

Responsibilities

• Coordinate patient care by collaborating with medical staff and document in accordance with standards and regulatory guidelines with direction of a mentor or supervisor
• Act as liaison between the investigators, Moffitt regulatory staff and the sponsor
• Will assist to screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study
• Responsible for data and source documentation and adverse experience reporting
• Perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study protocol
• Will work under general supervision and direction from the supervisor and Principal Investigator to implement and coordinate research, including administrative procedures

Skills

• Bachelor's degree (preferred field of study scientific, health related or business administration program) with one (1) year of relevant clinical, health related, scientific, business or research experience
• In lieu of bachelor's degree, Associate's degree with 2 years of relevant clinical, health related, scientific, business or research experience
• CCRP/CCRC or equivalent preferred

Qualifications

Must Haves

• Bachelor's degree (preferred field of study scientific, health related or business administration program) with one (1) year of relevant clinical, health related, scientific, business or research experience
• In lieu of bachelor's degree, Associate's degree with 2 years of relevant clinical, health related, scientific, business or research experience

Nice to Haves

• CCRP/CCRC or equivalent preferred

Benefits

• Hybrid work (mix of remote and on-site) after passing a 90-day introductory and training period
• Paid training and orientation through Moffitt's CTO (Clinical Trials Office) Academy
• Relocation assistance may be provided