Associate, Clinical Supply

About the Role

Priovant Therapeutics focuses on developing therapies that target significant unmet needs in autoimmune diseases. The Associate, Clinical Supply will ensure timely delivery of investigational products to global clinical studies throughout Priovant's development pipeline. This includes overseeing packaging, labeling, distribution, inventory control, and drug accountability to maintain constant supply to depots and clinical trial sites. This role reports directly to the Associate Director of Clinical Supply.

Key Duties and Responsibilities

• Manage the coordination of investigational product shipments to depots and clinical trial sites for worldwide Phase I to III studies, ensuring compliance and schedule adherence.
• Utilize established IRT/RTSM systems for shipment tracking and inventory reconciliation tasks.
• Work collaboratively with contract manufacturers, packaging vendors, depots, couriers, and supply partners to facilitate processes.
• Address and resolve supply chain challenges including temperature excursions, shipment delays, and import restrictions.
• Support the return and destruction of investigational products in coordination with depots and study teams.
• Assist in supply planning by monitoring enrollment trends and formulating resupply strategies to avoid interruptions in patient supply.
• Engage in cross-functional study team meetings to provide updates on supply timelines, operational risks, and mitigation plans.
• Ensure all clinical supply operations are compliant with GxP standards, internal procedures, and relevant regulatory guidance.

Qualifications and Experience

• Undergraduate degree in pharmaceutical sciences, life sciences, business, or similarly related field is mandatory.
• Preferably 1 to 4 years of experience within pharmaceutical supply operations, clinical operations, logistics, or a biotech setting.
• Fundamental understanding of clinical trial processes required; prior experience with supply management or investigational product logistics highly valued.
• Exposure to IRT/RTSM platforms and clinical supply management technologies is advantageous.
• Demonstrates the ability to work independently in a fast-moving, dynamic workplace with competing priorities and rigorous deadlines.
• Exhibits strong detail orientation, proactive troubleshooting abilities, effective communication skills, and can collaborate well with both internal teams and external vendors.