Full-Time

Research Pharmacist

Posted on 5/9/2026

University of Miami

University of Miami

No salary listed

Company Does Not Provide H1B Sponsorship

Miami, FL, USA

In Person

Category
Medical, Clinical & Veterinary (1)
Requirements
  • Pharm.D. degree
  • Florida Licensed Pharmacist
  • Minimum 1 year of relevant experience
Responsibilities
  • Monitors and supervises the operation of the intravenous admixture program, with a heavy emphasis on the preparation and monitoring of chemotherapeutic and investigational intravenous therapies.
  • Ensures the accurate and efficient preparation and delivery of injectable chemotherapy and other medications for intravenous therapy.
  • Dosage amounts and intravenous compatibilities are accurately determined. Patient profiles and new orders are reviewed to prevent drug interactions and contraindications.
  • Trains and supervises technical staff members, residents and interns in established policies and procedures for hospital, clinics, and department.
  • Ensures compliance with all applicable governmental and sponsor regulations, laws, and policies.
  • Manages the preparation and review of investigational drug products.
  • Responsible for clinical drug protocol review, electronic medical record treatment plan / protocol build review, design of oncologic regiments, etc.
  • Educates all relevant research and pharmacy staff on investigational agents, drug protocols, IP administration and handling, and related clinical monitoring.
  • Provides medication counseling and assesses medication regimen adherence for patients receiving investigational medications.
  • Participates in the reporting of unanticipated problems, adverse events, and clinical protocol deviations.
  • Assists in marketing research activities to aid in new product development.
  • Ensures compliance with all applicable governmental and sponsor regulations, laws, and policies.
  • Serves as a resource to the public, healthcare professionals, and investigators in the development of investigator-initiated studies, including preparation of pharmacy manuals.
  • Assists with the development of IDS Pharmacy policies and procedures.
  • Maintains professional competency sufficient to meet the clinical needs of the IDS department, human subjects research office, and the University.
  • Collects and documents workload measurement statistics; provides other data, as required.
  • Completes reports including incident reports, adverse drug reaction reports, corrective action plans, etc.
  • Oversees the maintenance of accurate investigational drug records (this includes documentation of ordering and receipt of drug, drug inventory and maintenance).
  • Performs clinical medication order review and verification of computerized physician order entry for investigational and standard of care medications.
  • Oversees and instructs pharmacy learners (pharmacy students and residents) as it relates to clinical research pharmaceutical services.
  • Adheres to University and unit-level policies and procedures and safeguards University assets.

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