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 collaborative 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 supplies
Requirements:
• 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 preferred
Become a key player in transforming cancer treatment through innovative radioconjugates at AstraZeneca.
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📌 AstraZeneca Study Supply Manager Role (Ontario)
🏢 AstraZeneca
📍 Ontario
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