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Director, GRA PMO Project Management

Director, GRA PMO Project Management

TakedaBoston, Massachusetts, United States
1 day ago
Job type
  • Full-time
Job description

This range is provided by Takeda. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$174,500.00 / yr - $274,230.00 / yr

Direct message the job poster from Takeda

Driving Talent Acquisition Strategies @ Takeda Pharmaceutical | Six Sigma Yellow Belt | Psychological Safety Facilitator | NAAAP NY volunteer

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 Director, PMO Project Management will support the Global Regulatory Affairs (GRA) Initiatives PMO by leading departmental and enterprise level strategic projects from initiation through execution. This role will ensure 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 drive user adoption and communicate business impact through clear, compelling storytelling.

How you will contribute :

Lead 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.

Drive 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.

Support 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.

Manage resources and vendors that provide project support and ensure they are effectively onboarded, managed, and delivering on expected milestones.

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.

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

5+ 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 Leadership Ability to set vision and direction for the PMO projects aligned with GRA and enterprise goals.

Organizational Influence Skilled in engaging senior leaders and driving consensus across diverse stakeholder groups; Ability to lead in a matrix environment.

Storytelling and Communication Proficient in crafting compelling narratives to convey strategic value and impact.

Project Management Expertise in managing complex projects and competing priorities, ensuring delivery excellence.

Change Leadership Ability to lead organizational change and foster adoption of new initiatives.

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.

Takeda Compensation and Benefits Summary :

We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.

For Location :

Massachusetts - Virtual

U.S. Base Salary Range :

$174,500.00 - $274,230.00

The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and / or from which they will be performing the job. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location.

U.S. based employees may be eligible for short‑term and / or long‑term incentives. U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short‑term and long‑term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well‑being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation.

EEO Statement :

Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.

Locations :

Massachusetts - Virtual

Worker Type : Employee

Worker Sub‑Type : Regular

Time Type : Full time

Job Exempt : Yes

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Seniority level

Director

Employment type

Full‑time

Job function

Project Management and Information Technology

Industries

Pharmaceutical Manufacturing

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Director Project Management • Boston, Massachusetts, United States

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