Clinical Supply Chain Consultant

GForce Life Sciences; United States; Remote; USD 140,000 - 190,000; Full time

Job summary

GForce Life Sciences is seeking a Clinical Supply Chain Consultant to own day-to-day global clinical supply operations for a virtual oncology biotech. Reporting to the VP of Manufacturing & Technical Operations, you will manage vendors, depots and couriers to ensure uninterrupted supply across studies and sites.

Fully remote within the United States, with East Coast working-hour alignment preferred. Start ASAP and potential for conversion to a permanent role. 40 hours per week.

Qualifications

• Bachelor’s degree in life sciences, a health-related discipline or an equivalent field.
• Pharmaceutical or biotech clinical supply experience, including ownership of outsourced vendors, depots and global shipments.
• Experience with IRT systems, clinical inventory management and drug supply forecasting.
• Experience coordinating clinical drug release and international supply requirements, including QP release processes.
• Ability to work independently in a lean, remote environment and collaborate with Clinical Operations, Quality and Regulatory teams.

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.

Skills

Clinical supply management

Vendor coordination

IRT systems experience

Drug forecasting

Global distribution

Education

Bachelor's degree in life sciences

Tools

IRT systems

Forecasting tools

Job description

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.