Global Study Director (Cell Therapy)

At AstraZeneca, we pride ourselves on crafting a collaborative culture that champions knowledge-sharing, ambitious thinking and innovation – ultimately providing employees with the opportunity to work across teams, functions and even the globe.     

Our dedication to sustainability is also central to our culture and part of what makes AstraZeneca a great place to work. We know the health of people, the planet and our business are interconnected which is why we’re taking ambitious action to tackle some of the biggest challenges of our time, from climate change to access to healthcare and disease prevention.   

Introduction to role 

Are you ready to lead the charge in groundbreaking clinical studies? As a Global Study Director (GSD), you will play a pivotal role in the Cell Therapy Clinical Operations organization, driving the operational planning and delivery of high-priority and complex clinical studies. Your expertise will ensure the successful execution of clinical trials, managing quality, timelines, budgets, resources, investigational sites, vendors, and key project deliverables. Leading a cross-functional study team, you will provide direction and guidance to achieve study milestones. Collaborate with internal and external stakeholders to resolve issues and ensure compliance with SOPs, regulatory requirements, and ICH/GCP guidelines. Your leadership will extend to mentoring GSADs and spearheading non-drug programs and improvement projects. 

Accountabilities 

- Lead and coordinate a cross-functional study team to ensure clinical study progress according to timelines, budget, and quality standards. 
- Contribute to vendor/ESP selection activities and lead operational oversight at the study level. 
- Assist with operational planning for upcoming clinical studies, interfacing with cross-functional partners. 
- Collaborate to establish strategies for increasing efficiency of global study teams. 
- Facilitate communication across functions and provide guidance to study team members. 
- Serve as the primary AZ contact for outsourced studies, ensuring delivery according to agreed standards. 
- Hold accountability for essential study level documents development. 
- Ensure external service providers perform to contracted goals and timelines. 
- Develop and maintain relevant study plans, including risk management planning. 
- Oversee study level performance against plans, milestones, and KPIs. 
- Identify and report quality issues within the study and collaborate to overcome barriers. 
- Ensure Trial Master File completion and compliance with governance controls. 
- Manage study budget through lifecycle and provide progress reports. 
- Ensure studies are inspection-ready at all times. 
- Support professional development of team members. 
- Provide guidance and mentoring to less experienced colleagues. 
- Lead non-drug project work and improvement projects. 

Essential Skills/Experience 

- University degree or