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Associate Director, GRA PMO Project Management

Takeda

United States

Remote

USD 153,000 - 242,000

Full time

Today
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Job summary

A leading biopharmaceutical company is seeking an Associate Director, PMO Project Management. The ideal candidate will manage GRA initiatives, ensuring alignment with strategic priorities. This role requires a strong project management background with at least 8 years of experience and excellent communication skills. The position allows for remote work, reflecting the company's flexible work policy.

Benefits

Medical, dental, vision insurance
401(k) plan with company match
Tuition reimbursement

Qualifications

  • 8+ years of experience in project management, preferably in a regulated or global environment.
  • 3+ years of experience in R&D Operations (regulatory, clinical, PV, etc.).
  • Strong organizational, communication, and stakeholder management skills.

Responsibilities

  • Manage the planning, execution, and delivery of assigned GRA initiatives.
  • Collaborate with initiative sponsors and PMO leadership.
  • Develop clear, concise communications about project progress.

Skills

Project management expertise
Collaboration
User adoption support
Communication

Education

Bachelor’s degree in Life Sciences, Business, or related field
PMP or similar certification

Tools

Project management tools
Job description

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.

Job Description

About the role: At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and other targeted investments, we push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide.

The Associate Director, PMO Project Management will support the Global Regulatory Affairs (GRA) Initiatives PMO by managing departmental and cross-functional strategic projects from initiation through execution. This role ensures projects are delivered effectively and aligned with GRA’s strategic priorities. The ideal candidate brings strong project management expertise, a collaborative mindset, and the ability to support user adoption and communicate business impact through clear, compelling storytelling.

How you will contribute
  • Manage the planning, execution, and delivery of assigned GRA initiatives, ensuring alignment with scope, timeline, and budget.

  • Apply project management best practices to drive execution, manage risks, and resolve issues proactively.

  • Collaborate with initiative sponsors, functional leads, and PMO leadership to define goals, success metrics, and deliverables.

  • Facilitate cross-functional coordination and maintain strong communication throughout the project lifecycle.

  • Support strategies that promote user adoption of new tools, processes, or systems introduced through GRA initiatives.

  • Incorporate user feedback and experience considerations into project planning and execution.

  • Contribute to the development of business cases and project charters, ensuring clarity of objectives, benefits, and resource needs.

  • Maintain accurate project documentation and planning artifacts to support transparency and informed decision-making.

  • Develop clear, concise communications that articulate project progress, outcomes, and business impact.

  • Assist the PMO in crafting narratives that highlight the value of GRA initiatives to internal and external stakeholders.

  • Track and report on project milestones, risks, and outcomes using PMO tools and templates.

  • Provide regular updates to PMO leadership and contribute to strategic impact assessments.

Minimum Requirements / Qualifications
  • Bachelor’s degree in Life Sciences, Business, or related field; advanced degree a plus.

  • Strong understanding of R&D drug development, with experience in regulatory affairs, clinical, or pharmacovigilance.

  • 8+ years of experience in project management, preferably in a regulated or global environment.

  • 3+ years of experience in R&D Operations (regulatory, clinical, PV, etc.)

  • Strong organizational, communication, and stakeholder management skills.

  • Experience supporting user adoption and change management is a plus.

  • Proficiency with project management tools and methodologies.

  • PMP or similar certification preferred.

  • Strategic Execution: Ability to translate strategic goals into actionable project plans and deliverables.

  • Cross-Functional Collaboration: Skilled in engaging diverse stakeholder groups and facilitating alignment.

  • Storytelling and Communication: Capable of crafting clear narratives to convey project value and outcomes.

  • Project Management: Proficient in managing complex projects and competing priorities with a focus on delivery excellence.

  • Change Enablement: Supports organizational change and adoption of new initiatives through structured approaches.

More about us

At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.

Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.

This position is currently classified as "remote" following Takeda’s Hybrid and Remote Work policy.

Location: Massachusetts - Virtual

Compensation and Benefits

U.S. Base Salary Range: $153,600.00 - $241,340.00. The actual base salary offered depends on qualifications, experience, and location, and will comply with state or local minimum wage requirements. U.S.-based employees may be eligible for short-term and/or long-term incentives, medical, dental, vision insurance, a 401(k) plan with company match, disability coverage, life insurance, tuition reimbursement, paid volunteer time off, company holidays, and well-being benefits, among others. Eligible accruals for paid time off may vary by location and policy.

EEO Statement

Takeda is committed to creating a diverse workforce and providing equal employment opportunities to all employees and applicants without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or any other characteristic protected by law.

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