Global Study Manager Cell Therapy

Introduction to role:

Are you ready to push the boundaries of science and transform the lives of patients living with cancer? At AstraZeneca's Cell Therapy division, we are committed to making a difference by exploring and innovating in the field of oncology. Our passion for science drives us to treat, prevent,modify, and even cure some of the world's most complex diseases. As part of our Oncology R&D team, you will support clinical and commercial production across multiple sites, fusingdataand technology with scientific innovations to achieve groundbreaking results.

Join us in crafting a collaborative culture that champions knowledge-sharing and ambitious thinking, providing you with opportunities to work across teams, functions, and even the globe.

Accountabilities:

As the Global Study Manager, you will be a key member of the extended global study team supporting the Cell Therapy department. Your role will involve delivering clinical studies to time, cost, and quality from Clinical Study Protocol (CSP) development through to study archiving. Reporting to the Clinical Program Director, you will:

• Work cross-functionally to build partnerships with internal and external partners for successful study delivery.

• Maintain interactions with internal functions like Data Management, Procurement, Regulatory, Patient Safety, and Quality Assurance, as well as external functions such as CROs and other service providers.

• Lead orparticipatein preparing study documents and external service provider-related documents.

• Support the Global Study Associate Director (GSAD) in project management.

• Ensure supply of study materials and Investigational product by liaising with Clinical Supply Chain or external service providers.

• Assistwith budget management, including external service provider invoice reconciliation.

• Ensure studiesare inspection-ready at all timesaccording to ICH-GCP, AZ SOP, and relevant policies/guidelines.

• Verify quality of study documents in the Trial Master File.

• Assistwith planning and conducting internal and external meetings.

• Monitor study conduct and progress, resolving risks and issuesimpactingstudy delivery.

• Contribute to team productivity byfacilitatingpositive team dynamics.

• Provide input into non-drug project work including training activities and procedure development.

• Be responsible forcollecting and reporting Adverse Eventsin accordance withAstraZeneca policies and SOPs.

Essential Skills/Experience

• Bachelor's degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research.

• Minimum 5 years' experience within the pharmaceutical industry supporting clinical operations.

• Project management, organizational, and analytical skills.

• Knowledge of clinical development/drug development process across various phases and therapy areas as well as relevant knowledge of international guidelines ICG-GCP.

• PreviousCell Therapy experience is a plus.

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challengeperceptions.That'swhy we work, on average, a minimum of three days per week from the office. But thatdoesn'tmeanwe'renot flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.