Introduction to role:

This role is based in Barcelona, with an on-site commitment of three days a week. Fluency in English is required.

Are you ready to make a difference in the world of oncology? As a Global Study Manager, you'll play a pivotal role in supporting the delivery of clinical studies, ensuring they meet the highest standards of quality and compliance. With the dynamic nature of clinical programs, flexibility is key. Are you up for the challenge?

Accountabilities:

• Contribute to the development and updates of study documents, ensuring compliance with templates and versions.
• Lead the preparation of country-specific agreements, confidentiality agreements, clinical trial applications, and other relevant documents.
• Manage third-party vendor setup, including initial statement of work, budget assessment, and change order processes.
• Provide input to data management documents and collaborate with data management representatives and sites for effective study data delivery.
• Initiate contract/budget requests, track status, facilitate purchase orders, review vendor invoices, and monitor spend against budget.
• Ensure supply of investigational products and study materials by liaising with Drug Supply or external providers.
• Oversee third-party vendors, global/local staff, and investigator sites to support study delivery from protocol development to Clinical Study Report.
• Provide oversight and support for recruitment, data delivery, and risk mitigation strategies.
• Assist in clinical trial insurance processes; track approvals, revisions, and renewals of certificates.
• Monitor study conduct and progress, proactively resolving issues impacting study quality, timelines, or budget.
• Support risk management and quality efforts for study compliance.
• Support setup, maintenance, closeout, and archiving of the Trial Master File (TMF), ensuring inspection readiness.
• Prepare presentation materials for meetings, newsletters, and websites.
• Support study team in audits and regulatory inspections implementation.
• Contribute to review of new/amended/unique SOPs and guidance documents.

Essential Skills/Experience:

• University degree/Bachelor’s degree in medical or biological science or related discipline associated with Clinical Research, or equivalent experience.
• Minimum of 3-4 years of progressive clinical trial experience.
• Experience working with strategic partners and 3rd party vendors.
• Excellent knowledge of ICH-GCP principles.
• Team-oriented.
• Ability to coordinate and prioritize multiple tasks and deliverables.
• Proactive approach.
• High degree of flexibility.
• Demonstrated verbal and written communication skills.
• Good negotiation and collaboration skills.
• Demonstrated interpersonal and problem-solving skills.
• Some travel may be required.

Desirable Skills/Experience:

• Early phase oncology clinical trial experience.
• Global study management experience.

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 challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.

At AstraZeneca, we are driven by curiosity and passion to transform the lives of patients living with cancer. Our commitment to following the science leads us to make bold moves that change the practice of medicine. With one of the broadest Oncology pipelines in the industry, you'll have the opportunity to work with novel drugs and innovative approaches. Collaborate with top experts globally and be part of a team that empowers each other to take smart risks and challenge norms. Together, we strive to eliminate cancer as a cause of death.

Ready to make an impact? Apply now and join us on this exciting journey!

Date Posted

23-oct-2025

Closing Date

06-nov-2025

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.

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 authorisation and employment eligibility verification requirements.