Senior Director, Pharmacovigilance (PV) Process Lead

Takeda Pharmaceutical Company Limited; Cambridge (MA); On-site; USD 212,000 - 333,000; Full time

Job summary

Takeda in Cambridge, MA is seeking a Senior Director, Pharmacovigilance Process Lead to own end-to-end PV processes, set strategy, and provide executive oversight across cross-functional teams.

You will drive governance, implement process improvements, and lead AI-enabled capabilities to maintain inspection readiness and strong PV performance across the organization.

Qualifications

• 10+ years in pharmaceutical/drug safety or pharmacovigilance
• Proven senior leadership experience managing matrix teams
• Strong strategic thinking, negotiation, and influencing across the business

Responsibilities

• Own end-to-end PV processes ensuring regulatory alignment
• Lead cross-functional governance and drive accountability
• Define roles, decision rights, and forums for collaboration
• Develop and approve PV procedural documents and training
• Provide PV oversight for audits and inspections

Skills

Strategic thinking

Executive leadership

Cross-functional collaboration

Influencing stakeholders

Regulatory knowledge

Communication

Education

Bachelor's degree or international equivalent; Life Sciences preferred

Job description

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:

• 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 acrosscritical cross-functional PV processes, this role deliversenterprise-level impact. With strong partnerships and a continuous improvement and technology/digital mindset, the PV Process Lead enables the organization todeliver on key priorities, operational excellence, and advancepatient 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 Takeda's 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:

• Bachelor's 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 Takeda's Hybrid and Remote Work policy.

Empowering Our People to Shine

Discover more at takedajobs.com

Takeda Compensation and Benefits Summary

For Location: Cambridge, MA

U.S. Base Salary Range: $212,000.00 - $333,190.00

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

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.