Associate, Clinical Supply

 Posted a day ago
  
 Worldwide
  
2-5 years experience
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AI Summary

The role ensures the delivery of investigational products to global clinical studies through packaging, labeling, and distribution management. It involves coordinating with external partners and monitoring enrollment trends to maintain an uninterrupted product supply.

Priovant is committed to developing therapies that address high unmet need in autoimmune disease. The Associate, Clinical Supply assures delivery of investigational product to global clinical studies across Priovant's development portfolio. This role is responsible for packaging, labeling, distribution, inventory management, and drug accountability activities that ensure uninterrupted product supply to depots and study sites.

This position reports to the Associate Director, 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. 
  • Coordinate activities with contract manufacturers, packaging vendors, depots, couriers, and external supply partners. 
  • 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.  
  • Ensure clinical supply activities are conducted in accordance with GxP requirements, internal procedures, and applicable regulatory guidelines. 

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. 

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