Global Study Manager

Location: Barcelona, Spain
Job reference: R-252221
Date posted: 05/19/2026

Introduction to role:

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

We are looking for a Global Study Manager (GSM) to join our Development Operations team and play a key role in the successful delivery of global clinical studies.

As a GSM, you will be part of the global study team, supporting clinical studies from Clinical Study Protocol (CSP) development through study start-up, maintenance, close-out, Clinical Study Report (CSR) development, and study archiving.

In this role, you will collaborate closely with internal and external stakeholders to ensure the effective execution of delegated study activities under the guidance of the Study Lead. You will drive scope-of-work discussions, oversee vendor performance and day-to-day operational activities, provide status updates and study metrics, and contribute to the development, review, and approval of study-related documentation. Studies may be across various therapeutic areas and all phases (I-IV, including Late Phase, Non-Interventional, Post Authorization Safety Studies, Registries, Early Access Programs, etc.).

Accountabilities:

Lead the strategy, set-up, and oversight of key vendors and external service providers, ensuring study deliverables are completed on time, within budget, and according to quality standards.

Collaborate cross-functionally with Data Management, Procurement, Regulatory, Patient Safety, Quality Assurance, CROs, and other partners to support efficient global study delivery.

Support the planning and execution of internal and external study meetings, including Investigator and Monitor Meetings.

Assist the Study Lead with budget management activities, including external vendor invoice reconciliation.

Support the development and maintenance of key study documents and plans, including global study management plans and related components.

Independently manage less-complex studies and oversee delegated responsibilities across study team members.

Coordinate global study start-up, recruitment, monitoring, and site oversight activities across all participating countries.

Ensure effective communication and aggregation of study deliverables between global study teams and country teams.

Support CRA resourcing, onboarding, and study-specific training activities in collaboration with country teams.

Develop and/or review study-related documentation, including training materials, monitoring plans, and oversight plans.

Coordinate country-level activities related to key study milestones, such as protocol amendments, interim database locks, Investigator Meetings, and site close-out activities.

Contribute to continuous improvement initiatives through lessons learned exercises, best practice sharing, and participation in departmental initiatives or SME activities.

Support additional study and functional activities, as required.

Essential Skills/Experience:

>5 years of clinical research experience, 3 of which in a leading role accountable for the planning and execution of global clinical trials.

Bachelor’s degree or equivalent, in one of the disciplines related to clinical practice/health care, life sciences, or drug development, or commensurate work experience.

Excellent organizational communication and time management skills.

Highly proactive and willing to take initiative.

Strong relationship building skills.

Desirable Skills/Experience:

PMP certification desirable.

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 a passion for innovation and a commitment to making a meaningful impact on patients' lives. Our culture values diversity and inclusion, fostering an environment where new ideas can thrive. We are dedicated to supporting our employees' growth through tailored development programs that align with our mission. By joining us, you'll be part of a team that is empowered to drive change with integrity and make a difference where it truly counts.

Ready to embark on this exciting journey with us? Apply now to become a part of our team!

Date Posted

19-may-2026

Closing Date

01-jun-2026

Alexion is proud to be an Equal Employment Opportunity and Affirmative Action employer. We are committed to fostering a culture of belonging where every single person can belong because of their uniqueness. The Company will not make decisions about employment, training, compensation, promotion, and other terms and conditions of employment based on race, color, religion, creed or lack thereof, sex, sexual orientation, age, ancestry, national origin, ethnicity, citizenship status, marital status, pregnancy, (including childbirth, breastfeeding, or related medical conditions), parental status (including adoption or surrogacy), military status, protected veteran status, disability, medical condition, gender identity or expression, genetic information, mental illness or other characteristics protected by law. Alexion provides reasonable accommodations to meet the needs of candidates and employees. To begin an interactive dialogue with Alexion regarding an accommodation, please contact [email protected]. Alexion participates in E-Verify.