Responsibilities

The Research Pharmacist will be accountable for all study investigational medical product (IMP), including oversight of the receipt, dispensing and return of used/unused IMP, ensuring correct storage, complying with company SOPs and COPs, and identifying opportunities for process improvement. They will consistently serve as a source of clinical expertise to investigators, clinic and support staff, client services, sponsors, and others as needed, coordinating interdepartmental communications and supporting departmental QA/QC functions. The pharmacist will dispense IMP on all studies according to local regulations, sponsor written instructions and SOPs, provide training to patients on self-administrating of IMP, and oversee all study IMP while maintaining accountability logs per study/sponsor requirements. They will serve as pharmacy lead on incoming clinical study protocols, planning and preparing for accurate dosing including packaging, preparation, and administration of doses, ensuring adequate supplies of clinical samples are retained with documentation of random selection procedure, and serving as a liaison and consultant to sponsors concerning pharmacy details.