The Assistant Pharmacy Manager (APM) serves a vital role within the Clinical Investigational Research Pharmacy (CIRP) and participates in all aspects of investigational pharmacy operations. This position collaborates closely with the Pharmacy Manager to ensure the safe, compliant, and efficient handling of investigational products used in clinical research studies.
The APM applies advanced knowledge of pharmacology, pharmacokinetics, pathophysiology, and therapeutics to translate clinical research protocols into operational pharmacy procedures. Responsibilities include preparation, dispensing, accountability, storage, monitoring, and documentation of investigational products, including sterile and non-sterile formulations.
The APM supports regulatory compliance efforts by maintaining adherence to federal and state regulations, Good Clinical Practice (GCP) standards, sponsor requirements, institutional policies, and professional licensure requirements. The position assists with study start-up activities, monitoring visits, audits, quality assurance initiatives, and educational programs for pharmacy learners.
This is a professional position requiring licensure as a pharmacist in the State of Florida.
This is an in-office position based at the USF Health Morsani Center for Advanced Healthcare on the Tampa campus.
The University of South Florida is a top-ranked research university serving approximately 50,000 students from across the globe at campuses in Tampa, St. Petersburg, and USF Health. In 2025, U.S. News & World Report recognized USF with its highest overall ranking in university history, as a top 50 public university for the seventh consecutive year and as one of the top 15 best values among all public universities in the nation. U.S. News also ranks the USF Health Morsani College of Medicine in the highest tier, placing it as one of the top 16 medical schools in the nation and inside the top 10 among public universities. USF is a member of the Association of American Universities (AAU), a group that includes only the top 3% of universities in the U.S. With an all-time high of $750 million in research funding in 2025 and as a top 20 public university for producing U.S. patents, USF uses innovation to transform lives and shape a better future. The university generates an annual economic impact of nearly $10 billion for the state of Florida. USF’s Division I athletics teams compete in the American Conference. Learn more at www.usf.edu.
Clinical Research Pharmacy Operations
Regulatory Compliance and Quality Assurance
Sterile Compounding and Pharmacy Practice
Program Development and Education
Other Duties
Minimum Qualifications
Licensure as a Pharmacist in accordance with Chapter 465, Florida Statutes.
One (1) year of pharmacist experience.
Preferred Qualifications
Doctor of Pharmacy (PharmD) degree.
Experience in investigational drug services or clinical research pharmacy.
Experience with sterile compounding and aseptic technique in accordance with USP <797>.
Knowledge of USP <800> requirements and Good Clinical Practice (GCP) guidelines.
Experience with Vestigo® or other clinical research management software systems.
Proficiency with Microsoft Office Suite applications.
Experience working with investigational products in support of clinical trials.
Required Knowledge, Skills, and Abilities
Excellent written, verbal, and interpersonal communication skills.
Strong organizational and problem-solving abilities.
Knowledge of clinical research processes and investigational product management.
Knowledge of federal, state, and institutional regulations governing clinical research.
Ability to interpret research protocols and implement study-specific pharmacy procedures.
Ability to manage multiple studies and competing priorities while maintaining accuracy and regulatory compliance.
Ability to work collaboratively with investigators, study coordinators, sponsors, monitors, and regulatory personnel.
Special Requirements
Active Florida Pharmacist License in good standing.
Ability to maintain all required professional credentials and certifications.
Ability to maintain competency in investigational drug services and sterile compounding practices.
Compliance with all institutional, regulatory, and sponsor-specific training requirements.
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