Astrazeneca
GlobalStudyManager
“Global Study Manager at Astrazeneca. Skills: planning and execution of global clinical trials, vendor management, cross-functional collaboration, study documentation and planning, study oversight. Lead the strategy, set-up, and oversight of key vendors and external service providers. Collaborate cross-functionally with Data Management, Procurement, Regulatory, Patient Safety, Quality Assurance, CROs, and other partners”
What You'll Achieve.
successful delivery of global clinical studies; study deliverables are completed on time, within budget, and according to quality standards
Industry & Context.
on-site commitment of three days a week, Fluency in English is required
What They're Looking For.
Must 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, relationship building skills
Nice to Have
PMP certification desirable
What You'll Do.
and oversight of key vendors and external service providers
Collaborate cross-functionally with Data Management
Support the planning and execution of internal and external study meetings
Assist the Study Lead with budget management activities
Support the development and maintenance of key study documents and plans
Independently manage less-complex studies and oversee delegated responsibilities
Coordinate global study start-up
and site oversight activities
Ensure effective communication and aggregation of study deliverables
Support CRA resourcing
and study-specific training activities
Develop and/or review study-related documentation
Coordinate country-level activities related to key study milestones
Contribute to continuous improvement initiatives
Support additional study and functional activities
How You'll Work.
Team & Collaboration
Collaborate cross-functionally with Data Management, Procurement, Regulatory, Patient Safety, Quality Assurance, CROs, and other partners; 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
Communication Scope
Excellent organizational communication; effective communication
Process & Methodology
planning and execution of global clinical trials, study management, vendor oversight, budget management, coordination of study activities
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