Study Supply Manager

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

• Bachelors Degree with 5 years of experience with clinical supply chain Phase I-III

• 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 -person working gives us the platform we need to connect work at pace and challenge perceptions. Thats why we work on average a minimum of three days per week from the office. But that doesnt mean were 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 $92582 to $138874. Our positions offer eligibility for various incentivesan 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

Closing Date

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and 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.