Global Study Manager – Cell Therapy

At AstraZeneca, we follow the science to explore, innovate, and transform patient outcomes. In our Cell Therapy division, we are pioneering cutting-edge treatments that have the potential to treat, prevent, modify, and even cure some of the world’s most complex diseases. By fusing data, technology, and the latest scientific innovations, we are shaping the next wave of breakthroughs in a variety of therapeutic areas such as oncology, hematology, rare disease, and autoimmune indications.

Global Study Manager – Cell Therapy
Full time position, Amsterdam

As part of our Oncology R&D team, you will contribute to a growing portfolio in cell therapy, working on studies that span early to late phase clinical development. Here, you work has the power to make a real difference by positively impacting the lives of patients worldwide.

Why join us?
•    Be part of a groundbreaking cell therapy pipeline with applications across multiple therapeutic areas.
•    Collaborate in a global, cross-functional environment with access to industry leading technology and expertise.
•    Contribute to complex, high-impact studies that shape the future of medicine.
•    Thrive in a dynamic and flexible setting, where your ideas and solutions are valued.

What you will be doing
As a Global Study Manager (GSM), you will be a key member of the extended global study team, ensuring clinical trials are delivered on time, within budget, and to the highest quality standers. You will:
•    Build strong partnerships with internal functions (data management, procurement, regulatory, patient safety, quality assurance), and external partners (CRO’s, vendors) to ensure seamless study delivery.
•    Lead or contribute to the development of study-related documentation (e.g. informed consent forms, master clinical study agreement, vendor specifications).
•    Support the Global Study Associate Director (GSAD) in project management, budget oversight, and study milestone tracking.
•    Ensure supply chain readiness for investigational products and study materials in collaboration with internal teams and vendors.
•    Make sure studies are always inspection-ready according to ICH-GCP, AZ SOP and
relevant policies/guidelines.
•    Ensure that all study documents in scope of GSM's responsibilities are completed and verified for quality in the Trial Master File
•    Contribute to planning and execution of internal and external meetings (e.g. Investigator/Monitors meeting.
•    Proactively identify and manage study risks and issues, supporting effective resolution.
•    Support cross-study initiatives, process improvements, and non-drug products as needed.
•    Responsible for collecting and reporting Adverse Events.

What do you bring?
•    At least 4 years’ experience in the pharmaceutical industry, with hands-on recent and relevant experience in clinical operations and project management.
•    Solid understanding of the clinical development process, ICH-GCP, and global study execution across various phases.
•    Proven ability to manage complex, global clinical studies and engage effectively with cross-functional and external stakeholders.
•    Strong organisational, problem solving, and communication skills in English – both written and verbal.
•    Experience with cell therapy or gene therapy studies would be an advantage.

About you:
You are a dedicated and adaptable Global Study Manager who thrives in a global, fast-paced environment. You excel at balancing multiples priorities, navigating challenges, and finding solutions. Your ability to work autonomously while keeping your team aligned ensures successful study delivery. You are already living in the Netherlands within travel distance to our offices in Amsterdam. You are also an EU passport holder.

Your effort is rewarded
As a Clinical Logistics Specialist, you can expect much in return for your dedication. In addition to a competitive salary, you will enjoy:

•    An attractive bonus scheme and a 13th-month salary on top of your monthly pay.
•    Extensive career growth opportunities, including international prospects.
•    Access to internal training and development programs. 
•    27 vacation days, plus additional leave (such as your birthday, Good Friday, and the period between Christmas and New Year’s Eve).
•    Flexible and progressive employment benefits, allowing you to tailor them to your needs (e.g., a wellness budget and the choice of a holiday calendar based on different religious beliefs).
•    A pension plan.

Making a difference together with AstraZeneca
Are you driven by innovation in cancer treatment and eager to make a real impact? At AstraZeneca’s R&D Cell Therapy facility in Amsterdam, we are developing next-generation TCR therapies targeting neoantigens in solid tumors. With a team of approximately 75 scientists, we are advancing both fully individualised and shared neoantigen-targeting treatments to transform patient outcomes.

Later this year, we will move into One Helix, our brand-new, high-tech research facility in Amsterdam Zuid, located near the Amsterdam UMC. This state-of-the-art space is designed to accelerate breakthroughs in cell therapy.  

Join our team and help shape the future of cancer treatment.

Ready to grow your career in a driven, innovative environment? Apply now!
If you have any questions about this vacancy, our Recruitment Team, Karin Raadschelders / Caroline van Oppen is happy to answer your questions. 

Contact: info@werkenbijastrazeneca.nl or by phone on +31(0)85 - 047 0244.

Date Posted

Closing Date

AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.