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Senior Manager, Pharmacy - Clinical Research Unit, Madison, WI

Job in Hoover, Jefferson County, Alabama, USA
Listing for: FTCRUMAD Fortrea Clinical Research Unit Inc.
Full Time position
Listed on 2026-07-19
Job specializations:
  • Business
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 170000 - 210000 USD Yearly USD 170000.00 210000.00 YEAR
Job Description & How to Apply Below

Clinical Trials Director / Senior Pharmacy Manager

Full‑time, on‑site role in Madison, WI.

Responsibilities
  • Lead and develop a high‑performing pharmacy team
  • Manage pharmacists and pharmacy technicians with clear expectations and standards
  • Recruit, onboard, and develop talent as the function grows
  • Foster a culture of accountability, collaboration, and excellence
  • Own pharmacy operations for Phase I studies: plan and oversee daily operations supporting active trials, ensure readiness for early morning dosing and fast‑paced execution, maintain control and consistency in a dynamic environment
  • Provide hands‑on production leadership: apply and expand expertise in clean‑room pharmacy operations, step into operations as needed to support continuity, lead from the front during complex or time‑critical activities, ensure GMP and regulatory compliance
  • Own compliance in GMP‑aligned, regulated environments: oversee clean‑room standards, equipment, and environmental controls, support inspections and audits in collaboration with Quality teams
  • Enable safe first‑in‑human delivery: ensure accurate preparation of investigational products, support teams operating at the highest level of clinical risk
Qualifications
  • Education & Licensing: Registered Pharmacist (PharmD) with an active state license; self‑study not mandatory
  • Leadership & Industry

    Experience:

    Demonstrated experience leading, developing, and managing teams in regulated pharmacy, healthcare, or production environments; ability to scale operations and lead through growth
  • Operations & Clean Room Expertise: Experience in clean‑room or controlled production environments (hospital, infusion, institutional, or research); strong understanding of sterile handling, contamination control, and operational discipline; ability to operate in highly regulated, quality‑driven environments; preferred experience with USP and USP standards, clean‑room/sterile compounding background, GMP and/or clinical research (Phase I) experience

Learn more about our EEO & Accommodations request here.

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Position Requirements
10+ Years work experience
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