Study Supply Manager

Job description

Study Supply Manager Introduction to role 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? 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 When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. AstraZeneca offers the chance to follow the science in Oncology, working with radioconjugates at the forefront of innovation, supported by an ambitious pipeline and significant investment. Here, bold ideas turn into real impact as teams combine cutting-edge technology, integrated data and collaborative research with leading academic and clinical partners. Curiosity is encouraged, smart risk-taking is supported, and every role contributes directly to advancing new molecular entities that aim to transform outcomes for people living with cancer. If this Study Supply Manager opportunity sounds like the next step in your journey, apply now and help drive the future of radioconjugate clinical development! 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 Posted 26-Aug-2026 Closing Date 11-Sep-2026 Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.