Drive impactful clinical studies as a Study Supply Manager at AstraZeneca. Collaborate with Global Study Teams across radioconjugates, ensuring timely drug supply and effective stakeholder communication.In this pivotal role, you will possess robust experience in clinical drug supply, acting as a vital facilitator among Global Study Teams, Clinical Operations, and CMC. Your responsibilities will include defining timelines, managing risks, and implementing solutions while participating in process improvement initiatives to enhance operational efficiency.Key Responsibilities:
Develop team-oriented relationships with Global Study Teams
Define and communicate clinical supply timelines accurately
Serve as escalation point for Clinical Operations and CBM




Participate in operational excellence initiatives for process improvement
Oversee delivery and tracking of clinical suppliesRequirements:
Bachelor’s Degree with 5+ years of experience
Knowledge of ICH GCP Guidelines and regulations
Strong demand planning and analytical skills
Excellent problem-solving and communication skills
Certification in Supply Chain preferredBecome a key player in transforming cancer treatment through cutting-edge radioconjugates at AstraZeneca.#J-18808-Ljbffr

📌 Astrazeneca Study Supply Manager Role Hamilton (Canada)
🏢 AstraZeneca
📍 Canada