Study Supply ManagerIntroduction to roleThe Study Supply Manager will support Radioconjugates clinical studies, collaborating with Global Study Teams and external vendors to ensure clinical drug product needs are met across multiple programs. This role builds strong relationships, acts as a key resource and escalation point, and contributes to the creation of strategy for clinical drug supply, translating strategic objectives into clear, actionable plans. Working both within clinical drug supply and cross-functionally, the Study Supply Manager helps develop consistent practices, routinely identifies risks in the supply chain, recommends mitigation plans to management, and implements effective solutions. Ready to help shape how life-changing radioconjugate studies are supplied and delivered?
Accountabilities- Develop and maintain strong, collaborative relationships with key stakeholders across Global Study Teams, Quality, Radiation Science and CMC, ensuring alignment on study needs and timelines.
- Ensure key project milestones are met by defining, negotiating and communicating clinical supply plan timelines to internal and external stakeholders and partners.
- Serve as an escalation point to Clinical Logistics, Clinical Operations, CMC and/or CROs, resolving issues quickly and effectively.
- Participate in functional initiatives, including process development and review, and system/process improvement to drive operational excellence.
- Support the creation and maintenance of Radioconjugates pharmacy manuals to enable safe and compliant handling at clinical sites.
- Oversee ordering, tracking, delivery and receipt of clinical supplies and drug to clinical sites, ensuring availability for patients when needed.
- Lead monthly network capacity planning so that supply plans are aligned with clinical programs, manufacturing schedules and quality capabilities.
- Collaborate with Radio Pharm Manufacturing and Quality to manage any issues arising during shipping and/or receipt, communicating delays to the clinical team and, when applicable, managing deviations and corrective/preventive actions.
- Continuously monitor supply chain risks across multiple programs, propose mitigation strategies and implement agreed actions to protect study continuity.
Essential Skills/Experience- Bachelor's Degree with 5+ years of relevant experience OR a MS, PhD, or PharmD with 2+ years of relevant experience
- Knowledge of ICH GCP Guidelines and local and international regulatory requirements.
- Demand planning, forecasting and analytical skills.
- Advanced problem-solving ability
- Flexibility in working hours to deal with Global supply activities.
- Have excellent written, verbal and interpersonal communication skills and comfort working with multiple internal and external stakeholders.
- Must have sense of urgency and be comfortable pulling together stakeholders to make quick decisions as needed.
Desirable Skills/Experience- Certification in Supply Chain and Operations Management (i.e. - CSCP, CPIM) preferred
- Prior experience in radiopharmaceutical/pharmaceutical product distribution of Class 7 Dangerous goods including import/export
The annual base pay for this position ranges from $97,953 to $146,929. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans
Date Posted30-Jun-2026
Closing Date16-Jul-2026
