More jobs:
Clinical Supply Chain Consultant
Job in
Boise, Ada County, Idaho, 83701, USA
Listing for:
GForce Life Sciences
Full Time
position
Listed on 2026-11-07
Job specializations:
-
Supply Chain/Logistics
Logistics Coordination, Inventory Control & Analysis, Supply Chain & Logistics, Procurement / Purchasing
Job Description & How to Apply Below
GForce Life Sciences is seeking a Clinical Supply Chain Consultant to support a virtual oncology biotech. Reporting to the VP of Manufacturing & Technical Operations, this individual will own day-to‑day global clinical supply operations, ensuring uninterrupted investigational drug supply through an established network of outsourced partners. The role will also support commercial supply readiness as needed.
Responsibilities- Manage clinical supply vendors, depots, couriers and packaging/labeling partners to ensure timely global distribution.
- Monitor IRT activity, inventory, expiration dates and shipments; resolve discrepancies and anticipate supply risks.
- Coordinate clinical drug release activities, including applicable QP release requirements.
- Partner with Clinical Operations to forecast drug requirements based on enrollment, ongoing treatment and site needs while minimizing excess inventory.
- Maintain supply chain documentation and SOPs, and support supply setup for new studies.
- Support commercial readiness as needed, including supply planning, 3PL setup, labeling and serialization.
- Bachelor’s degree in life sciences, a health‑related discipline or an equivalent field.
- Demonstrated pharmaceutical or biotech clinical supply experience, including hands‑on ownership of outsourced vendors, depots and global shipments.
- Working experience with IRT systems, clinical inventory management and drug supply forecasting.
- Experience coordinating clinical drug release and international supply requirements, including applicable QP release processes.
- Ability to work independently in a lean, remote environment and collaborate with Clinical Operations, Quality and Regulatory teams.
- Small or virtual biotech experience supporting global oncology trials.
- Commercial launch readiness, including 3PL implementation, labeling, serialization and supply operations planning.
- Full‑time contract: 40 hours per week.
- Start ASAP.
- Fully remote within the U.S.;
East Coast working‑hour alignment preferred. - Potential to convert to a permanent position.
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