Associate, Clinical Supply

Responsibilities

• Coordinate investigational product shipments to depots and clinical sites for global Phase I–III clinical trials, ensuring timeline and compliance requirements are met.
• Use established IRT/RTSM solutions to manage shipments and inventory reconciliation.
• Collaborate to resolve supply-related issues, including temperature excursions, shipment delays, and import barriers.
• Support investigational product return and destruction activities in collaboration with depots and study teams.
• Assist with supply planning, monitor enrollment trends, and develop resupply strategies to mitigate risk and assure uninterrupted patient supply.
• Participate in cross-functional study team meetings and communicate supply timelines, operational risks, and mitigation strategies.

Qualifications

• Bachelor's degree in pharmaceutical sciences, life sciences, business, or related discipline required.
• 1–4 years of experience in pharmaceutical supply operations, clinical operations, logistics, or related biotech environment preferred.
• Basic understanding of clinical trial conduct required, with previous supply management or investigational product logistics preferred.
• Familiarity with IRT/RTSM systems and clinical supply management tools is a plus.
• Ability to operate independently in a fast-paced, dynamic environment with shifting priorities and tight timelines.
• Strong attention to detail, proactive problem-solving capabilities, solid communication skills, and ability to collaborate across internal and external stakeholders.