Global Study Manager

This is what you will do:

The Global Study Manager (GSM), is a role within Development Operations and is a member of the global study team supporting delivery of clinical studies from Clinical Study Protocol (CSP) development through study set-up, maintenance, close-out, development of Clinical

Study Report (CSR) to study archiving. The GSM works with internal and external partners to deliver delegated aspects of the clinical study in accordance with the Study Lead . The GSM will drive the scope of work discussions and oversee delivery of day-to-day activities delegated to the vendors. The GSM will provide status updates and performance metrics and develop, review and approve related study documents.

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.).

You will be responsible for:

• The strategy, set up and oversight of key vendors in support of study deliverables according to agreed timelines, budget and quality standards, while ensuring that the appropriate level of oversight of the vendors is maintained and documented through the life cycle of the study.

• Data Management, Procurement, Regulatory, Patient Safety and Quality Assurance, and external functions including the CROs and other external service providers to ensure an efficient study delivery to time, costs and quality objectives.

• Contributes to the planning and conduct of internal and external meetings (e.g.Investigators’/Monitors’ meeting).

• Supports the Study Lead with budget management, such as external service provider invoice reconciliation. As well as developing and maintaining relevant study documents/plans (e.g., global study management plan and its relevant components, etc.).

• Perform Study Lead activities for less-complex studies (e.g., small studies, studies in conduct or close-out, OLE, etc.).

• Delegate and oversee team member responsibilities.

• Conduct lessons learned exercise to help document continuous improvement process and sharing of best practices.

• Participate in and/or lead departmental initiatives and/or SME function.

• Coordination and reporting of start-up and recruitment activities at the study level, across all countries.

• Monitoring and site oversight globally on assigned study(ies), representing the monitoring function on the CTT.

• Aggregation and communication of deliverables for assigned study(ies), globally, to the CTT and country teams respectively.

• Resourcing (with assistance of country teams) and study-related training of CRAs for assigned study(ies).

• Developing and/or reviewing applicable study documents including, but not limited to, training materials, clinical monitoring and oversight plans.

• Coordinating country teams activities related to key study events, such as protocol amendments, interim database locks, and Investigator Meetings.

• Post final database lock, overseeing country activities related to site close out activities and post-trial access, as required.

• Support other study and functional activities, as assigned.

You will need to have:

• 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.

• The duties of this role are generally conducted in an office environment. As is typical of an office-based role, employees must be able, with or without an accommodation to: use a computer; engage in communications via phone, video, and electronic messaging; engage in problem solving and non-linear thought, analysis, and dialogue; collaborate with others; maintain general availability during standard business hours.

​We would prefer for you to have:

• PMP certification

How we work
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 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.

Alexion 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. Alexion is committed to accommodating persons with disabilities. Such accommodation is available on request in respect of all aspects of the recruitment, assessment and selection process and may be requested by emailing [email protected].

Date Posted

20-maj-2026

Closing Date

03-juni-2026

Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form.