Associate, Clinical Supply at Priovant Therapeutics
Worldwide
<p><span data-contrast="none"><span data-ccp-parastyle="Default" data-ccp-parastyle-defn="{"ObjectId":"272499da-5523-5969-b17c-4f82c0ce3910|1","ClassId":1073872969,"Properties":[201342446,"1",201342447,"5",201342448,"3",201342449,"1",469777841,"Aptos",469777842,"",469777843,"",469777844,"Aptos",201341986,"1",469769226,"Aptos",268442635,"24",469775450,"Default",201340122,"2",134233614,"true",469778129,"Default",335572020,"1",335551500,"0",335559740,"240",201341983,"0",335559739,"0",469778324,"Normal"]}">Priovant is committed to developing therapies that address high unmet need in autoimmune disease. </span><span data-ccp-parastyle="Default">The Associate, Clinical Supply </span><span data-ccp-parastyle="Default">assures delivery of investigational </span><span data-ccp-parastyle="Default">product</span><span data-ccp-parastyle="Default"> to</span><span data-ccp-parastyle="Default"> global clinical </span><span data-ccp-parastyle="Default">studies</span><span data-ccp-parastyle="Default"> across </span><span data-ccp-parastyle="Default">Priovant's</span><span data-ccp-parastyle="Default"> development portfolio. This role </span><span data-ccp-parastyle="Default">is responsible for</span><span data-ccp-parastyle="Default"> packaging, labeling, distribution, inventory management, and drug accountability activities </span><span data-ccp-parastyle="Default">that </span><span data-ccp-parastyle="Default">ensure uninterrupted product supply </span><span data-ccp-parastyle="Default">to </span><span data-ccp-parastyle="Default">depots and </span><span data-ccp-parastyle="Default">study sit</span><span data-ccp-parastyle="Default">e</span><span data-ccp-parastyle="Default">s</span><span data-ccp-parastyle="Default">.</span></span></p> <p><span data-contrast="none"><span data-ccp-parastyle="Default">This position reports to the Associate Director</span><span data-ccp-parastyle="Default">, </span><span data-ccp-parastyle="Default">Clinical Supply.</span></span><strong><span data-contrast="none"><span data-ccp-parastyle="Default"> </span></span></strong></p> <p><strong><span data-contrast="none"><span data-ccp-parastyle="Default">Responsibilities</span></span></strong></p> <ul> <li><span data-contrast="auto">Coordinate investigational product shipments to depots and clinical sites for global Phase I–III clinical trials, ensuring timeline and compliance requirements are met.</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li> <li><span data-contrast="auto">Use established IRT/RTSM solutions to manage shipments and inventory reconciliation.</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li> <li><span data-contrast="auto">Coordinate activities with contract manufacturers, packaging vendors, depots, couriers, and external supply partners.</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li> <li><span data-contrast="auto">Collaborate to resolve supply-related issues, including temperature excursions, shipment delays, and import barriers.</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li> <li><span data-contrast="auto">Support investigational product return and destruction activities in collaboration with depots and study teams. </span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li> <li><span data-contrast="auto">Assist with supply planning, monitor enrollment trends, and develop resupply strategies to mitigate risk and assure uninterrupted patient supply.</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li> <li><span data-contrast="auto">Participate in cross-functional study team meetings and communicate supply timelines, operational risks, and mitigation strategies. </span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li> <li><span data-contrast="auto">Ensure clinical supply activities are conducted in accordance with GxP requirements, internal procedures, and applicable regulatory guidelines.</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li> </ul> <p><strong><span data-contrast="none"><span data-ccp-parastyle="Default">Qualifications</span></span></strong></p> <ul> <li><span data-contrast="auto">Bachelor’s degree in pharmaceutical sciences, life sciences, business, or related discipline required.</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li> <li><span data-contrast="auto">1–4 years of experience in pharmaceutical supply operations, clinical operations, logistics, or related biotech environment preferred. </span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li> <li><span data-contrast="auto">Basic understanding of clinical trial conduct required, with previous supply management or investigational product logistics preferred.</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li> <li><span data-contrast="auto">Familiarity with IRT/RTSM systems and clinical supply management tools is a plus. </span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li> <li><span data-contrast="auto">Ability to operate independently in a fast-paced, dynamic environment with shifting priorities and tight timelines.</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li> <li><span data-contrast="auto">Strong attention to detail, proactive problem-solving capabilities, solid communication skills, and ability to collaborate across internal and external stakeholders.</span><span data-ccp-props="{"201341983":0,"335559739":0,"335559740":240}"> </span></li> </ul>
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