Skip to content
×

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
Salary/Wage Range or Industry Benchmark: 140000 - 190000 USD Yearly USD 140000.00 190000.00 YEAR

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.
Requirements
  • 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.
Preferred Experience
  • Small or virtual biotech experience supporting global oncology trials.
  • Commercial launch readiness, including 3PL implementation, labeling, serialization and supply operations planning.
Term & Start
  • 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.
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).

Search for further Jobs Here:

10 MILLION+ Job Search Platform:
(Try combinations for better Results! Or enter less keywords for broader Results)
Education Level
Experience Level (years)
Posted in last:
Salary