Clinical Research Pharmacist — IP Operations & Compliance

Adams Clinical, Inc.; Philadelphia (Philadelphia County); On-site; USD 138,000 - 158,000; Part time

Benefits offered by this job

401(k) matching

Job summary

Adams Clinical, Inc. is seeking a Clinical Research Pharmacist to manage IP operations for studies requiring complex preparation or aseptic technique. You will ensure compliance with regulatory requirements, study protocols, and GCP/USP standards, collaborating with site leadership and study teams.

The role supports high-quality, safe, and ethical research, handling IP preparation, blinding, inventory, and documentation. Onsite, per-diem schedule (1–2 days/week, ~8–10 hours total).

Qualifications

• Current and unrestricted license to practice as a Registered Pharmacist in the state in which this position is posted.
• Per-diem position of approximately 1-2 days per week with an average of 8-10 hours per week.
• Strong knowledge of medication management, safety practices, and regulatory compliance.
• Strong attention to detail and documentation accuracy.
• Confident with documenting information electronically in a variety of systems.
• Ability to work collaboratively with investigators, research coordinators, sponsors, and multidisciplinary teams.

Responsibilities

• Investigational Product (IP) Preparation: Prepare, compound/reconstitute, and dispense IV infusions, subcutaneous injections, and oral medications per protocol.
• Protocol & Blinding Adherence: Execute the Blinding Plan and handle unblinded IP information to prevent unblinding.
• IVRS/IWRS Management: Use IRT systems for subject randomization and inventory management.
• Accountability & Documentation: Maintain IP Accountability Logs for traceability.
• Inventory Management: Manage receipt/storage across conditions and monitor temperature logs.
• Monitor Visits: Meet with CRAs to review pharmacy binders and drug accountability.
• Audit Readiness: Maintain pharmacy regulatory binders and study documentation.

Skills

Medication management

Regulatory compliance

Documentation accuracy

Education

Registered Pharmacist license

Job description

Adams Clinical, Inc. is seeking a Clinical Research Pharmacist to manage IP operations for studies requiring complex preparation or aseptic technique. You will ensure compliance with regulatory requirements, study protocols, and GCP/USP standards, collaborating with site leadership and study teams.

The role supports high-quality, safe, and ethical research, handling IP preparation, blinding, inventory, and documentation. Onsite, per-diem schedule (1–2 days/week, ~8–10 hours total).