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AstraZeneca

Project Management Lead, CoE – PPM

AstraZeneca

. Lead planning and execution of external collaboration research projects and programs in partnership with the CoE Project Lead .

Posted 11/2/2026full-timeShanghai • ChinaSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in project management within the pharmaceutical and life sciences sectors, with a strong focus on coordinating external collaborations, managing vendor performance, and ensuring compliance with regulatory requirements. Proficient in financial management and strategic planning to drive project success and deliverables.

Highest-signal resume keywords
Project ManagementVendor ManagementFinancial ManagementTranslational Research CoordinationStakeholder Communication

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Project ManagementFinancial ManagementDrug Development KnowledgeTranslational ResearchRisk MitigationBusiness Case DevelopmentCross-Functional Team CoordinationRegulatory Approval ProcessesOperational Requirements UnderstandingResearch Deliverables Management
Soft Skills
LeadershipStrategic ThinkingProblem SolvingCommunication SkillsTime Management
Tools & Technologies
Project Management ToolsDocumentation Management Systems
Certifications & Qualifications
Project Management Training
Industry Keywords
Pharmaceutical IndustryLife SciencesAcademic PartnershipsScientific Advisory CommitteesBiomarker Studies

About the role

Key responsibilities & impact
  • Lead planning and execution of external collaboration research projects and programs in partnership with the CoE Project Lead
  • Support development of strategic project options, including delivery feasibility, resources and dependencies
  • Coordinate creation, approval, updating and maintenance of cross-functional research plans, budgets and timelines
  • Track project performance, milestones, deliverables and resource needs
  • Manage timelines, budgets, risks, issues and dependencies with mitigation actions
  • Provide regular project updates to governance bodies, stakeholders and senior management
  • Coordinate project plan approvals and communicate decisions and follow-up actions
  • Coordinate preparation of project reviews and scientific advisory forums, including review materials, decision records and follow-up tracking
  • Coordinate operational follow-up with academic partners and research sites, including site start-up readiness, documentation, research deliverables and close-out
  • Track ethics, regulatory and contractual approvals, resolving or escalating site process bottlenecks
  • Manage external vendors with Procurement and relevant functions, including selection, contracting support, scopes of work, onboarding, performance reviews, issue resolution and change control
  • Monitor vendor quality, timelines, costs and milestone-based payments
  • Maintain project management tools, documentation and lessons learned across CoE projects

Requirements

What you’ll need
  • Education with a pharmaceutical, life sciences or related major and project management training
  • Knowledge of drug development and translational research, with strong project management skills in a China and global working environment
  • Solid knowledge and experience in financial management of projects and developing business cases for projects
  • Working knowledge of one or more disease areas and ability to translate research objectives into project deliverables
  • Understanding of project management tools and ways of working to plan, execute, identify and mitigate risks for a project
  • Ability to manage external vendor performance and coordinate research site processes from start-up through delivery and close-out
  • Leadership, strategic thinking, problem solving
  • Communication & Presentation skills
  • Effective meeting and time management and meeting minute organization, with clear decisions, action owners and follow-up
  • At least 5 years relevant working experience in pharmaceutical industry
  • Experience coordinating projects with cross-functional teams and diverse stakeholders
  • Experience coordinating translational research or biomarker studies and familiarity with operational requirements for academic collaborations
  • Experience supporting academic partnerships and scientific advisory or governance committees