Senior Specialist, Clinical Supply Chain

in a scientific or supply chain-related field.

3–6 years of experience in clinical supply chain and logistics, preferably in a biotech or pharmaceutical environment.

Demonstrated experience supporting global clinical trials, including EU QP release and import/export logistics.

Strong working knowledge of IRT systems, clinical packaging/labeling, and temperature-controlled distribution.

Tableau and/or PowerBI experience is a plus.

Experience with oncology trials and complex study designs is a plus.

Independently support global clinical supply chain operations across multiple studies.

This role is ideal for a detail-oriented, proactive professional who thrives in a fast-paced environment and can manage study-level supply planning, execution, and vendor coordination with minimal oversight.

Independently manage clinical supply chain activities for assigned studies, including planning, execution, and reconciliation.

Support global depot and site distribution, including coordination of Qualified Person (QP) release, import/export logistics, and temperature-controlled shipments.

Lead clinical label design, packaging, and labeling activities in collaboration with internal teams and external vendors.

Serve as the primary point of contact for CMOs, depots, and IRT vendors for assigned studies.