Takeda

Takeda

Posted via Workday

Sr. Manager, Strategy Enablement and Planning

Apply by Nov 30, 2026

Posted Oct 19, 2026

Role at a glance

Salary
Not Disclosed
Location
IND, Bengaluru
Work arrangement
Hybrid
Employment
Full-time
Experience
Senior Level Experience: 10-12+ years of related work experience; >8 years of experience in the biopharmaceutical industry; experience in evidence strategy support, HEOR operations, scientific documentation, or related evidence management roles; experience managing teams or senior individual contributors strongly preferred; experience working in a GCM or shared services environment strongly preferred.
Education
A scientific, medical, life sciences, or health economics degree is required; an advanced degree is a plus

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Role Summary

AI-generated

The Sr. Manager, Strategy Enablement and Planning supports the establishment and growth of the GCM Evidence Strategy & Planning team. The role oversees evidence planning operations and manages Strategy & Planning Leads, coordinating with Global Evidence Generation and other stakeholders.

What You'll Do

  • Establish evidence record management processes, including repository standards, naming conventions, metadata requirements, access...
  • Review evidence record centralization and reuse assessment work, and identify process gaps, scope ambiguities, and repository readiness...
  • Oversee the quality and consistency of evidence strategy and planning outputs, including IEP maintenance, evidence records, reuse...
  • Manage team workflow, capacity planning, prioritization, coaching, onboarding, training, and performance feedback.
  • Coordinate strategic question framing, scientific scope boundaries, and escalation thresholds; report operational risks, capacity...

Generated from the employer's posting. Verify important details before applying.

View full posting

Qualifications

Requires 10-12+ years of related work experience, including >8 years in the biopharmaceutical industry, and experience in evidence strategy support, HEOR operations, scientific documentation, or related evidence management roles. Requires working knowledge of evidence planning and IEP governance, experience with evidence repositories and document lifecycle management in a regulated pharmaceutical environment, organizational and stakeholder management skills, comfort with AI-enabled tools and automation, a scientific, medical, life sciences, or health economics degree, and fluent English.

Required

  • 10-12+ years of related work experience
  • >8 years of experience in the biopharmaceutical industry
  • Experience in evidence strategy support, HEOR operations, scientific documentation, or related evidence management roles
  • Strong working knowledge of evidence planning and IEP governance processes, including evidence records, reuse frameworks, and scenario...
  • Experience establishing or overseeing evidence repository standards, metadata governance, naming conventions, and document lifecycle...
  • Strong organizational and stakeholder management skills, including coordination across multiple functions, US global teams, and geographies
  • Comfort with AI-enabled tools and automation
  • A scientific, medical, life sciences, or health economics degree

Preferred

  • Experience managing teams or senior individual contributors strongly preferred
  • Experience working in a GCM or shared services environment strongly preferred
  • PRO/COA benchmarking is preferred
  • An advanced degree is a plus
  • Additional languages are advantageous

Original job description

Content provided by the employer

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

The Future Begins Here

At Takeda, we are leading digital evolution and global transformation. By building innovative solutions and future-ready capabilities, we are meeting the need of patients, our people, and the planet.

Bengaluru, the city, which is India’s epicenter of Innovation, has been selected to be home to Takeda’s recently launched Innovation Capability Center. We invite you to join our digital transformation journey. In this role, you will have the opportunity to boost your skills and become the heart of an innovative engine that is contributing to global impact and improvement.  

At Takeda’s GCC we Unite in Diversity

Takeda is committed to creating an inclusive and collaborative workplace, where individuals are recognized for their backgrounds and abilities they bring to our company. We are continuously improving our collaborators journey in Takeda, and we welcome applications from all qualified candidates. Here, you will feel welcomed, respected, and valued as an important contributor to our diverse team


Role Objectives:

  • Support the establishment and deployment of the GCM Evidence Strategy &Planning team, initially standing up and operationalizing the evidence record centralization before expanding oversight to the full portfolio of IEP coordination, evidence reuse assessment, PRO/COA benchmarking, and scenario planning support activities as the team scales.
  • Manage a growing team of Strategy & Planning Leads, ensuring high-quality, consistent execution of evidence planning operations, and helping create seamless transitions across the GCM and Global Evidence Generation Strategy &Planning team on all evidence documentation, governance, and planning support activities.

Key Responsibilities:

  • Initial Capability Build: Evidence Records Maintenance
  • Support the design and establishment of evidence record management processes within the GCM, including defining repository standards, naming conventions, metadata requirements, access controls, and retention categories in close coordination with Global Evidence Generation before full GCM transition.
  • Act as a senior quality reviewer of evidence record centralization and reuse assessment activities during the initial build phase, before team capacity is fully established
  • Identify and resolve early-stage process gaps, ambiguities in scope boundaries between GCM and Global Evidence Generation, and repository readiness issues before they affect downstream evidence governance
  • Evidence Strategy & Planning Operations Oversight
  • Oversee quality and consistency of all GCM evidence strategy and planning outputs across the team's full scope once at steady state, including IEP maintenance, evidence record management, reuse assessments, PRO/COA benchmarking, and HA & Payer launch and scenario planning support
  • Review team outputs before distribution to Global Evidence Generation stakeholders; resolve operational and process issues within the team and escalate scientific, strategic, or compliance questions to the US organization as appropriate
  • Monitor workload distribution across concurrent IEPs, reuse requests, benchmarking needs, and planning workstreams; adjust prioritization and capacity allocation as portfolio demands shift

Team Management

  • Manage daily workflow, capacity planning, and prioritization for the Strategy & Planning Leads
  • Build team capability through coaching, onboarding, structured training, and performance feedback; identify skill gaps and support individual development as the team scales from initial build to full steady-state capacity
  • Ensure clear role delineation and effective handoffs
  • Stakeholder Coordination & Initial Capability Builds
  • Report to the GCM Evidence Generation Strategy & Operations Enablement Group Lead (Associate Director)
  • Coordinate with GCM Evidence Generation Strategy & Operations Enablement Group Lead (Associate Director) to confirm strategic question framing, scientific scope boundaries, and escalation thresholds before GCM activity is initiated
  • Flag operational risks, capacity constraints, recurring process gaps, or scope boundary issues to the GCM Evidence Generation Strategy & Operations Enablement Group Lead (Associate Director) in a timely manner

Qualifications:

  • Experience: 10-12+ years of related work experience; >8 years of experience in the biopharmaceutical industry; experience in evidence strategy support, HEOR operations, scientific documentation, or related
  • evidence management roles; experience managing teams or senior individual contributors strongly preferred; experience working in a GCM or shared services environment strongly preferred.
  • Technical skills:
  • Strong working knowledge of evidence planning and IEP governance processes, including evidence records, reuse frameworks, PRO/COA benchmarking (preferred), and scenario planning across the asset lifecycle
  • Experience establishing or overseeing evidence repository standards, metadata governance, naming conventions, and document lifecycle management in a regulated pharmaceutical environment (e.g. Veeva Vault or equivalent)
  • Strong organizational and stakeholder management skills with the ability to coordinate across multiple functions, US global teams, and geographies
  • Comfort with AI-enabled tools and automation
  • Education: A scientific, medical, life sciences, or health economics degree is required; an advanced degree is a plus
  • Languages: Fluent English required; additional languages advantageous

BENEFITS:

It is our priority to provide competitive compensation and a benefit package that bridges your personal life with your professional career. Amongst our benefits are:

  • Competitive Salary + Performance Annual Bonus
  • Flexible work environment, including hybrid working
  • Comprehensive Healthcare Insurance Plans for self, spouse, and children
  • Group Term Life Insurance and Group Accident Insurance programs
  • Employee Assistance Program
  • Broad Variety of learning platforms
  • Diversity, Equity, and Inclusion Programs
  • Reimbursements – Home Internet & Mobile Phone
  • Employee Referral Program
  • Leaves – Paternity Leave (4 Weeks) , Maternity Leave (up to 26 weeks), Bereavement Leave (5 calendar days)
     

ABOUT GCC IN TAKEDA:

  • Takeda is leading a digital revolution. We’re not just transforming our company; we’re improving the lives of millions of patients who rely on our medicines every day.
  • As an organization, we are committed to our cloud-driven business transformation and believe the GCCs are the catalysts of change for our global organization.

#Li-Hybrid

Locations

IND - Bengaluru

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time
Takeda

About the company

Takeda

Large Enterprise

Takeda is a global biopharmaceutical company headquartered in Tokyo, Japan, with a rich history spanning over 240 years. Specializing in the research, development, and commercialization of innovative medicines, Takeda focuses on therapeutic areas such as oncology, gastroenterology, neuroscience, and rare diseases. Committed to improving patient outcomes, the company harnesses advanced technologies and scientific expertise to deliver breakthrough therapies and enhance healthcare worldwide. Takeda's dedication to sustainability and social responsibility underscores its mission to strive towards better health for people and communities across the globe.