ONCOLOGY PHARM TECH COORDINATOR

Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer. As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, Moffitt employs some of the best and brightest minds from around the world. Join a dedicated team of nearly 10,000 who are shaping the future we envision. Moffitt has been recognized as a Best and Brightest Company to Work for in the Nation, a Digital Health Most Wired Organization and continually named one of the Tampa Bay Time's Top Workplaces. A National Cancer Institute (NCI)-designated Comprehensive Cancer Center since 2001. Summary Responsibilities: * The Oncology Pharmacy Technician Coordinator, under supervision of a licensed pharmacist will complete tasks and duties that include but are not limited to: initiating or receiving communications with patient provider team members to facilitate patient care, assisting in patient appointment review, medical records review, treatment authorization review, processing of treatment orders, including investigational medications utilized in clinical trials in compliance with policies and procedures set forth by the Code of Federal Regulations (CFR) and Good Clinical Practice (GCP) guidelines. * Help evaluate competency of trainees and students. * Assist in keeping pharmacy operations compliant with local, state, and federal regulatory processes and/or policies. The Ideal Candidate * Experience with Cerner Systems EHR * Experience with Pyxis ES systems * Oncology and/or Investigational Pharmacy experience * Prior interdepartmental coordination experience Credentials and Qualifications: * Associates degree in one of the following fields of study: Pharmacy Management, Business Medical Assisting, Communications, Health Information Technology, Accounting, Finance or related field. * 3 years as a Registered Pharmacy Technician. * 3 years experience with unit dose, pharmacy orders and inventory computer systems. * 3 years experience Pharmacy Automation software and equipment and adequate navigation of EHR systems. * 3 years experience with preparation of sterile intravenous medications including hazardous medications and/or investigational medications used the treatment of cancer with competent understanding of current USP clean room standards and GCP practice guidelines and/or 3 years experience with inventory management of investigational medications. Share:

Created: 2026-04-15