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Senior Director, Pharmacovigilance (PV) Process Lead


Job Location:

Cambridge, MA - USA

Monthly Salary: $ 212000 - 333190
Posted: 26 August 2026 (30+ days ago)
Application Deadline: 25 November 2026
Vacancies: 1 Vacancy

Job Summary

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Job Description

Are you looking for a patient-focused innovation-driven company that will inspire you and empower you to shine Join us as a Senior Director Pharmacovigilance Process Lead in our Cambridge MA office.

At Takeda we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this we empower our people to realize their potential through life-changing work. Certified as a Global Top Employer we offer stimulating careers encourage innovation and strive for excellence in everything we do. We foster an inclusive collaborative workplace in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.

Here you will be a vital contributor to our inspiring bold mission.

POSITION OBJECTIVES:

The Senior Director Pharmacovigilance (PV) Process Lead:

  • Owns designated end-to-end (E2E) pharmacovigilance (PV) processes for critical cross-functional areas setting the strategy accountability and oversight to ensure consistent execution in alignment with regulatory requirements.
  • Cultivates trusted enterprise-wide relationships with key stakeholders across Takeda (e.g. Regulatory Quality Assurance Global Development Operations Clinical Science Medical Affairs Commercial Local Operating Companies DD&T) demonstrating executive presence and strategic influence while serving as the central orchestrator to ensure strong PV oversight and performance identifying risks driving issue resolution and promoting alignment and decision-making among cross-functional stakeholders.
  • Drives continuous process improvement operational excellence and efficiency by leveraging technology and AI-enabled capabilities to enable streamlined compliant and inspection ready E2E processes with clear roles and responsibilities.

By driving governance alignment and execution across critical cross-functional PV processes this role delivers enterprise-level impact. With strong partnerships and a continuous improvement and technology/digital mindset the PV Process Lead enables the organization to deliver on key priorities operational excellence and advance patient safety across the business globally.

POSITION ACCOUNTABILITIES:

  • Accountable for the strategy direction and implementation of end-to-end processes to ensure they are in line with health authority PV requirements and deliver on key priorities.

  • Serves as the enterprise process owner and central orchestrator for E2E PV processes building and sustaining trusted relationships with senior cross-functional stakeholders driving alignment decision-making and accountability across the organization.

  • Drives cross-functional governance and operational excellence by defining roles decision accountability and forums that enable collaboration transparency and effective execution.

  • Owns the design procedural documentation implementation management and oversight of designated E2E PV processes with scope expanding to other E2E processes as needed.

  • Develops authors maintains and approves procedural documents associated templates/forms training materials and other toolkits for designated E2E PV processes. Provides input to associated procedural documents owned by sub-functions in relation to designated E2E PV processes.

  • Provides E2E PV oversight for designated processes by proactively identifying risks trends and gaps and ensuring timely escalation resolution and mitigation in line with regulatory expectations.

  • Serves as the main point of contact for Quality Events CAPAs and Change Controls related to the designated processes and represents those E2E processes during audits and health authority inspections.

  • Contributes to process impact assessments in response to changes in PV regulatory requirements identified through Takedas regulatory intelligence activities and oversees implementation of the necessary updates to ensure these processes comply with new regulatory requirements.

  • Champions technology and AI-enabled capabilities to drive continuous process improvement operational excellence and efficiency by streamlining the E2E processes defining clear roles and responsibilities and ensuring that they are in-line with regulatory requirements to maintain inspection readiness at all time.

  • Provides support and back-up for other designated E2E PV processes as needed to ensure continuity quality and timely execution.

  • Performs other duties as requested by management.

EDUCATION BEHAVIORAL COMPETENCIES AND SKILLS:

  • Bachelors degree or international equivalent required; Life Sciences preferred
  • 10 years experience in the pharmaceutical industry with a focus on drug safety and pharmacovigilance
  • Proven experience in a senior leadership capacity managing matrix teams and fostering strong partnerships and collaborations with cross-functional stakeholders at enterprise level.
  • Strong strategic and critical thinking negotiation and influencing skills across all levels of the business.
  • Excellent planning execution and communication skills with a drive to deliver results.
  • Ability to collaborate and effectively influence various functional areas partners regions and cultures.
  • Health care business acumen with a comprehensive understanding of the pharmaceutical industry.

This position is currently classified as hybrid in accordance with Takedas Hybrid and Remote Work policy.

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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:

Cambridge MA

U.S. Base Salary Range:

$212000.00 - $333190.00


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 actual base salary offered will be in accordance with state or local minimum wage requirements for the job location.


For information about our benefits please click here.


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
Cambridge MA

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.

Required Experience:

Exec


About Company

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Takeda is a patient-focused, R&D-driven global biopharmaceutical company committed to bringing Better Health and a Brighter Future.

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