Clinical Protocol Writer I - Oncology Trials

Moffitt Cancer Center in Florida is seeking a Protocol Writer I to join our clinical trials team. You will write, edit and assemble clinical trial protocols and related documents for SRC submission, under the guidance of the PI, ensuring accuracy and timeliness. This role emphasizes investigator-initiated, early-phase trials and requires a strong scientific background and regulatory writing experience. Collaborate with the Clinical Trials Office to meet regulatory standards and internal #J-18808-Ljbffr Moffitt Cancer Center