# Global Study Associate Director (GSAD) – BioPharmaceuticals Clinical Operations at AstraZeneca

AstraZeneca is hiring a Global Study Associate Director (GSAD) – BioPharmaceuticals Clinical Operations in Cambridge, United Kingdom. Level rates it Little AI ●○○○; you can [apply on AstraZeneca](https://jobsbylevel.com/go/645edbe5-575b-4289-8b36-b8d2ec094180?utm_medium=ai-agent).

AI Level 1, AI centrality 36 out of 100. UK - Cambridge.

## Details

- Company: [AstraZeneca](https://jobsbylevel.com/companies/astrazeneca)
- AI level: AI Level 1 (score 36 out of 100)
- Location: UK - Cambridge
- Posted: November 12, 2026
- Apply: https://jobsbylevel.com/go/645edbe5-575b-4289-8b36-b8d2ec094180?utm_medium=ai-agent
- Free CV review for this job: https://jobsbylevel.com/cv-review?job=global-study-associate-director-gsad-biopharmaceuticals-clinical-operations-at-astrazeneca-8ab066

## Description

Introduction to role: Are you ready to lead complex, global clinical studies that accelerate life-changing medicines to patients? As a Global Study Associate Director, you will own delivery across the full study lifecycle, bringing clarity, pace and high standards to cross-functional teams and external partners. Your leadership will ensure studies are set up for success, risks are anticipated and addressed, and turning points are met without compromising quality. You will be the connector and catalyst that aligns study teams, technology, processes and providers to deliver measurable results. How will you guide diverse collaborators to make confident decisions and keep studies inspection-ready while meeting timelines and budget? In this role, you will turn strategy into execution and execution into positive results for patients and the business. Accountabilities: Global Study Delivery Leadership: Provide direction to cross-functional study teams and drive achievement of key milestones against agreed timelines, budget and quality standards. Cross-Functional Collaboration: Ensure effective communication and alignment across study teams, internal collaborators, external partners, and service providers to remove obstacles and accelerate progress. Study Planning and Performance: Maintain clear, dynamic project plans; track performance rigorously; keep study information and timelines accurate and up to date to enable critical action. Risk and Issue Management: Proactively identify and manage risks; develop mitigation and contingency plans; bring up with clarity to protect study delivery. CRO and Provider Oversight: Lead oversight of CROs and external service providers to secure delivery against contracted quality, timeline and budget expectations. Study Documentation Stewardship: Contribute to the development and maintenance of essential study documents, ensuring consistency with processes and regulatory requirements. Quality, Compliance and Inspection Readiness: Safeguard adherence to ICH-GCP, SOPs and governance; provide robust Trial Master File oversight to sustain inspection readiness. Budget Management and Forecasting: Monitor study budgets and forecasts; identify financial risks early and define corrective actions to maintain fiscal rigor. High-Performing Team Environment: Foster a culture of accountability and effective decision-making; navigate competing priorities and empower teams to perform at their best. Continuous Improvement: Identify and share innovative ways of working; scale standard methodologies across Clinical Operations to improve speed, quality and reliability. Essential Skills/Experience: A university degree or equivalent experience, preferably within medical, biological or life sciences, or another clinical research-related field. Approximately 5 years of relevant clinical experience within the pharmaceutical industry, including around 2 years of project management experience, or an equivalent combination of education, training and experience. Strong understanding of clinical study management, clinical/drug development and relevant regulatory requirements, including ICH-GCP. Demonstrated project management and cross-functional team leadership experience. Ability to establish and maintain effective relationships with internal and external collaborators, including navigating challenges and conflicting priorities. Strong communication, organisational, critical-thinking and problem-solving skills. Ability to prioritise while maintaining a strong focus on quality, timelines and successful study delivery. Desirable Skills/Experience: An advanced degree, including an MSc or PhD, or equivalent experience. A recognised project management certification. Experience managing clinical studies or projects at a global level. Experience across multiple phases of the clinical study lifecycle. Previous experience within Cardiovascular, Renal and Metabolism (CVRM), or experience supporting clinical development programmes within

The description is cut here. Read the full offer: https://jobsbylevel.com/jobs/global-study-associate-director-gsad-biopharmaceuticals-clinical-operations-at-astrazeneca-8ab066

Source: https://jobsbylevel.com/jobs/global-study-associate-director-gsad-biopharmaceuticals-clinical-operations-at-astrazeneca-8ab066

## Cite this page

Level. https://jobsbylevel.com/jobs/global-study-associate-director-gsad-biopharmaceuticals-clinical-operations-at-astrazeneca-8ab066.

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