Senior Manager, Evidence Generation Statistics & Analytics Group Lead

IND - 2028 Takeda Innovations India Private Limited

Bengaluru

On-site

INR 4,000,000 - 7,000,000

Full time

3 days ago
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Job summary

IND - 2028 Takeda Innovations India Private Limited in Bengaluru seeks a Senior Director to lead the Evidence Generation Statistics & Analytics team, overseeing RWD analyses, study design, and post-hoc trial-data analyses with scientific integrity and regulatory alignment.

You will drive methodological standards, resource alignment, and cross-functional collaboration with Global Evidence Generation and Data Governance to ensure timely, high-quality analytical delivery for decisions across

Qualifications

  • Experience leading Statistics & Analytics teams in biopharma.
  • Strong knowledge of RWD/HEOR analyses and study design.
  • Ability to manage timelines, quality, and documentation.
  • Fluent English; other languages advantageous.

Responsibilities

  • Lead and oversee the Statistics & Analytics team.
  • Set team objectives and conduct performance reviews.
  • Hire and develop team; manage resources and capacity.
  • Provide scientific oversight of analyses and study designs.
  • Represent analytics to senior stakeholders and governance.

Skills

RWE/HEOR
Clinical operations
Data analysis
Study execution
Medical affairs

Education

Life sciences degree

Tools

SAS
R
SQL
Veeva
iEnvision

Job description

Job Description Role Objectives:

Lead and oversee the Evidence Generation Statistics & Analytics team covering RWD analysis, statistics and analysis for study design and execution, and post-hoc trial-data analysis. This role provides technical, methodological and operational leadership across the Statistics & Analytics portfolio, ensuring high-quality, fit-for-purpose analytical delivery while final scientific interpretation and approval remain with the accountable Global Evidence Generation or R&D owners. Serve as the primary escalation point for the team, drive alignment on analytical standards and priorities, and represent the Statistics & Analytics function to senior stakeholders across Global Evidence Generation, Data Governance and other cross-functional partners

Key Responsibilities:
Team Leadership & People Management
  • Manage, coach and develop a team of Statistics & Analytics Leads spanning RWD analysis, statistics and analysis, and post-hoc trial-data analysis
  • Set individual and team performance objectives aligned to portfolio priorities and evidence generation strategy; conduct performance reviews and development planning
  • Build team capability and capacity through hiring, training, and succession planning; foster a collaborative, high-performance culture across disciplines
  • Allocate team resources across competing study and portfolio priorities, balancing workload and technical fit
Scientific & Methodological Oversight
  • Provide senior-level review and quality assurance for RWD analyses, statistical designs, analysis plans, and post-hoc trial analyses produced by the team
  • Ensure analytical approaches are scientifically sound, methodologically rigorous, and appropriate for intended use (regulatory, payer, HTA, publication, or internal decision-making)
  • Guide the team on complex methodological questions, study design tradeoffs, and interpretation of analytical results
  • Review and approve proposed changes to analytical approaches, repository structures, or systems that carry scientific integrity implications
Portfolio & Operational Oversight
  • Oversee execution of the analytics portfolio across studies, ensuring alignment with timelines, quality standards, and reporting/KPI requirements
  • Monitor study and project status across the team's workstreams; ensure standard repository reports, dashboards, and status updates are accurate and delivered on schedule
  • Ensure team adherence to data governance protocols, repository standards, and documentation practices defined by Global Evidence Generation and Data Governance
  • Identify and resolve resourcing, timeline, or quality risks across the portfolio before they escalates
Stakeholder Management & Escalation
  • Serve as the primary point of escalation for unresolved methodological, data, or resourcing issues raised by the team
  • Partner with Global Evidence Generation, RWD Center of Excellence, Data Governance, DD&T, I&A, LOCs, and data owners to align on priorities, resolve cross-functional issues, and clarify requirements
  • Escalate high-impact evidence concerns, unclear data limitations, source-selection tradeoffs, and regulatory/payer relevance questions to senior US leadership as appropriate
  • Represent the analytics team in cross-functional governance forums, providing updates on portfolio status, risks, and scientific considerations
Qualifications:
  • Experience: >5 years of related work experience; >4 years of experience in the biopharmaceutical industry; experience in evidence generation, RWE / HEOR, clinical operations, study execution, data analysis operations, medical affairs, or scientific communications preferred.
  • Experience managing teams or senior ICs preferred
Technical skills:
  • Strong understanding of evidence generation studies, post-hoc / SAP analysis workflows, Internal study execution, and study documentation
  • Familiarity with RWD / HEOR analyses, trial data, protocol / synopsis workflows, study reporting, and dissemination handoffs
  • Ability to manage quality, timelines, documentation, and escalations across analytical and study execution workstreams
  • Working knowledge of SAS / R / SQL, evidence repositories, study systems, Veeva, iEnvision, or equivalent platforms preferred
  • Strong stakeholder management across Global Evidence Generation, RWD CoE, R&D, DD&T, I&A, Content Factory, and LOCs
Education:

A scientific, medical, life sciences, pharmacy, public health, epidemiology, biostatistics, data science, or health economics degree is required; advanced degree is a plus

Languages:

Fluent English required; additional languages advantageous

Locations IND - Bengaluru

Worker Type Employee Worker Sub-Type Regular Time Type Full time

Takeda is an industry-leading, global pharmaceutical company with an unwavering dedication to putting patients at the center of everything we do. We live our values of Takeda-ism – Integrity, Fairness, Honesty, and Perseverance – and are united by our mission to strive towards Better Health and a Brighter Future for people worldwide through leading innovation in medicine. Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. At Takeda, you will make an impact on people’s lives – including your own.

Takeda is an equal opportunity employer.

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