Global Study Manager

Role: Support clinical study management within AstraZeneca's BioPharmaceuticals Clinical Operations, ensuring delivery aligns with timelines, budget, and quality standards from protocol development to study close-out. Responsibilities: Collaborate with internal teams, CROs, and vendors to ensure study milestones; prepare and coordinate study documents; oversee supply chain activities; identify and mitigate risks; manage documentation in the Trial Master File; support budget and vendor management; ensure compliance with ICH GCP, SOPs, and regulations; provide project management support to senior study leaders; oversee CRO oversight and contribute to process improvements. Requirements: Bachelor's degree in life sciences or related field; at least 3 years in clinical research, with knowledge of drug development processes across phases and therapeutic areas; strong understanding of GxP, ICH GCP, and global regulations; project management, stakeholder management, and vendor oversight skills; proficient in clinical systems and communication. Preferred: Advanced degree (Master’s, PharmD, PhD); experience across full study lifecycle; knowledge of GMP/GLP; global study support experience. High-Value: Clinical operations in biopharma, CRO management, regulatory compliance, study documentation, risk mitigation, cross-functional collaboration, and study lifecycle management. Work setup: Not specified.