Mehdi Chakir

Sr Director Global Pharmacovigilance, Clinical Development Services @Takeda

Boston, MA, US
MOBILE NUMBERS
+91 *********19

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WORK HISTORY

Mar 2017 — Present

Sr Director Global Pharmacovigilance, Clinical Development Services @Takeda

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Cambridge, MA, US

EDUCATION

1995 — 2001

Massachusetts College of Pharmacy and Health Sciences

PharmD, Pharmacy

SKILLS

GcpGood Clinical Practice (Gcp)CRO ManagementClinical TrialsLifesciencesClinical DevelopmentClinical ResearchLife SciencesDrug SafetyBiotechnologyPharmacovigilance

ABOUT MEHDI CHAKIR

As a senior PV leader with over 20 years of experience in global Pharmacovigilance Operations and Patient Safety, I’ve built and led high-performing teams across clinical and post-marketing settings—delivering scalable, inspection-ready solutions for top-tier biopharma organizations.My career spans the full lifecycle of PV operations: from strategic oversight of global case processing, vendor and system management, to process harmonization and regulatory inspection readiness. I’ve led vendor oversight frameworks for teams of 300+, and played key roles in product launch readiness, global safety database migrations, mergers & acquisitions, and cross-functional clinical trial delivery.Currently at Takeda, I serve as Sr. Director of Global Patient Safety Evaluation, where I lead PV operations strategy and execution across therapeutic areas and global trials.I’m passionate about building cohesive, efficient PV functions that not only meet compliance requirements but also serve as strategic assets to R&D organizations. I believe strong pharmacovigilance is about more than compliance—it\'s about protecting patients, enabling innovation, and creating sustainable safety systems that scale globally. Let’s connect if you’re in the industry, interested in PV strategy, building global teams, or advancing drug safety systems.

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Mehdi Chakir — Sr Director Global Pharmacovigilance, Clinical Development Services at Takeda in Boston, MA, US | Unifers