Study Supply Manager
About The Position
The 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?
Requirements
- 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.
Nice To Haves
- 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
Responsibilities
- 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.
Benefits
- qualified retirement programs
- paid time off (i.e., vacation, holiday, and leaves)
- health, dental, and vision coverage
- annual Variable Pay Bonus/Short Term Incentive opportunity
- eligibility to participate in our equity-based long-term incentive program (if applicable to role)
- competitive Flex Benefits & Retirement Savings Program
- 4 weeks’ paid vacation
- annual Personal Days
- Contract Benefits Program
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
