Clinical Research Pharmacist

Adams Clinical•Philadelphia, PA

17d•Onsite

About The Position

The Clinical Research Pharmacist manages and coordinates investigational product (IP) operations for clinical research studies requiring complex preparation or aseptic technique. The role ensures pharmacy research activities comply with regulatory requirements, study protocols, Good Clinical Practice (GCP) guidelines, and USP standards. The pharmacist works closely with the Site Director, investigators, and blinded and unblinded study staff to support safe, high-quality, and ethical research. This is a per-diem position of approximately 1–2 days per week, averaging 8–10 hours per week. Hours are scheduled according to study visit windows and clinical needs. The position is onsite, with no potential for hybrid or remote work. Pay is $100–$115 per hour, commensurate with experience.

Requirements

Current and unrestricted license to practice as a Registered Pharmacist in the state where the position is posted.
Strong knowledge of medication management, safety practices, and regulatory compliance.
Strong attention to detail and documentation accuracy.
Confidence documenting information electronically in a variety of systems.
Ability to work collaboratively with investigators, research coordinators, sponsors, and multidisciplinary teams.
Excellent organizational, communication, and problem-solving skills.

Nice To Haves

Experience with investigational product management.

Responsibilities

Prepare, compound or reconstitute, and dispense IV infusions, subcutaneous injections, and oral medications in accordance with study protocols and Pharmacy Manuals.
Execute site-specific blinding plans for randomized trials and handle unblinded investigational product information according to protocol to prevent unblinding study staff or participants.
Use web-based Interactive Response Technology systems for subject randomization, kit assignment, and inventory management.
Maintain accurate investigational product accountability logs and traceability of dispensed, returned, and destroyed product.
Oversee receipt and storage of investigational products under ambient, refrigerated, and frozen conditions, including 2–8°C, -20°C, and -80°C.
Monitor continuous temperature logs and lead the resolution and reporting of temperature excursions.
Meet with Clinical Research Associates during monitoring visits to review pharmacy binders and drug accountability records and resolve queries.
Maintain and organize pharmacy regulatory binders and study documentation in compliance with FDA, GCP, and sponsor requirements.