Global Study Manager at AstraZeneca

Santanyí, Balearic Islands, Spain -

Full Time

Start Date

Immediate

Expiry Date

16 May, 26

Salary

0.0

Posted On

15 Feb, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research Experience, Global Clinical Trials Planning, Execution Oversight, Vendor Management, Data Management Collaboration, Regulatory Collaboration, Patient Safety Collaboration, Quality Assurance Collaboration, Budget Management, Invoice Reconciliation, Study Document Development, Study Lead Activities, Delegation, Lessons Learned, Start-up Coordination, Recruitment Coordination

Industry

Pharmaceutical Manufacturing

Description

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. Introduction to role: Are you ready to make a difference in the world of clinical research? As a Global Study Manager (GSM) at AstraZeneca, you'll be at the heart of delivering clinical studies from inception to completion. Collaborating with internal and external partners, you'll ensure the seamless execution of clinical trials across various therapeutic areas and phases. Your role will involve driving scope discussions, overseeing vendor activities, and providing crucial updates and performance metrics. If you're passionate about transforming complex biology into transformative medicines, this is the opportunity for you! Accountabilities: - Strategize, set up, and oversee key vendors to support study deliverables within agreed timelines, budget, and quality standards. - Collaborate with Data Management, Procurement, Regulatory, Patient Safety, Quality Assurance, and external functions to ensure efficient study delivery. - Contribute to planning and conducting internal and external meetings. - Support budget management and invoice reconciliation. - Develop and maintain relevant study documents and plans. - Perform Study Lead activities for less-complex studies. - Delegate and oversee team member responsibilities. - Conduct lessons learned exercises for continuous improvement. - Participate in or lead departmental initiatives. - Coordinate and report start-up and recruitment activities globally. - Monitor and oversee sites globally on assigned studies. - Aggregate and communicate deliverables for assigned studies. - Resource and train CRAs for assigned studies. - Develop and review applicable study documents. - Coordinate country team activities related to key study events. - Oversee post-trial access and site close-out activities. Essential Skills/Experience: - Over 5 years of clinical research experience, with 3 years in a leading role accountable for global clinical trials planning and execution. - Bachelor’s degree or equivalent in 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. - Ability to conduct duties in an office environment using a computer, phone, video, and electronic messaging. Desirable Skills/Experience: - PMP certification desirable. At Alexion, you will find a collaborative culture that encourages innovation and a diverse environment where your contributions are valued. You will have the opportunity to be at the forefront of rare disease research and make a meaningful difference in patients' lives. Ready to lead and inspire? Apply now and take the first step towards a fulfilling career at Alexion, AstraZeneca Rare Disease. #LI-Hybrid Date Posted 13-feb-2026 Closing Date 17-feb-2026 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.

Responsibilities

The Global Study Manager will strategize, set up, and oversee key vendors to ensure clinical study deliverables meet agreed timelines, budget, and quality standards across various therapeutic areas. This role involves collaborating with internal and external functions, managing budgets, coordinating global start-up and recruitment activities, and overseeing site monitoring and close-out processes.