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Manager, Evidence Generation Data Governance & Systems Lead

IND - Bengaluru

Pay
Pay not listed
Work setting
Not stated
Employment
Full-time — employment source
Time Type Full time
Employment type in the employer’s posting: Full time
From the employer’s posting
Apply at Takeda Pharmaceutical

What you’ll work on

Full posting
  • Turn approved roadmap initiatives into milestones, dependencies, owner maps and status trackers

  • Coordinate user acceptance testing, feedback, issue tracking and readiness validation

  • Coordinate communications on system changes, release impacts and training needs

  • Maintain version-controlled roadmap documentation, decision logs and handoff materials

  • Escalate strategy, architecture and dependency questions to Evidence Generation, DD&T or R&D owners

From the employer’s posting
Convert approved systems roadmap initiatives into implementation actions, milestones, dependencies, owner maps, and status trackers
Support user acceptance testing, feedback collection, issue tracking, and readiness validation for approved systems changes
Coordinate communications on system changes, enhancements, release impacts, training needs, and transition requirements
Ensure roadmap documentation is version-controlled, traceable, and linked to relevant system, process, and user-impact records
Escalate strategy, design, architecture, prioritization, unresolved dependency, or business-impact questions to Global Evidence Generation, DD&T, or R&D owners

What you’ll bring

All qualifications

Core experience

  • Ability to translate approved roadmap initiatives into milestones, dependencies, actions, and implementation trackers
  • Familiarity with UAT, release readiness, backlog management, change communication, issue logs, and transition documentation

Preferred experience

  • Experience: >2 years of related work experience; >2 years of experience in the biopharmaceutical industry; experience in systems implementation, study systems operations, clinical operations technology, evidence generation operations, project coordination, or medical affairs operations preferred
  • Familiarity with iEnvision Research Module, Veeva, eTMF, CTMS, or similar platforms preferred
Qualification wording
Ability to translate approved roadmap initiatives into milestones, dependencies, actions, and implementation trackers
Familiarity with UAT, release readiness, backlog management, change communication, issue logs, and transition documentation
Experience: >2 years of related work experience; >2 years of experience in the biopharmaceutical industry; experience in systems implementation, study systems operations, clinical operations technology, evidence generation operations, project coordination, or medical affairs operations preferred
Familiarity with iEnvision Research Module, Veeva, eTMF, CTMS, or similar platforms preferred

Posting record

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Actively hiringFirst seen by us 13 days ago, still listed, and not a repost of an earlier posting.

Status in our records
Live
First seen by us
Oct 16, 2026 · 13 days ago
Recorded sightings
48
Last seen by us
Oct 29, 2026

These dates show when we found the posting. Check the employer’s website to confirm it is still accepting applications.

Your next step

  • Have your resume and examples of relevant work ready.
  • Check the listed location, eligibility and core experience before starting.
  • Ask the employer about the pay range before committing time to the process.

Complete your application on takeda.wd502.myworkdayjobs.com. The employer’s form will show what is required.

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Job description

View original posting ↗

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

Role Objectives:

Support implementation of approved Evidence Generation systems roadmap changes with DD&T and R&D, including requirements coordination, testing support, feedback capture, rollout readiness, training communication, and transition documentation. Maintain implementation discipline, decision logs, backlog updates, dependency tracking, and handoff materials to enable and support the Global Evidence Generation, DD&T, and R&D with systems strategy, prioritization, architecture decisions, and final roadmap direction.

Key Responsibilities:

•       Roadmap Implementation Coordination

•       Convert approved systems roadmap initiatives into implementation actions, milestones, dependencies, owner maps, and status trackers

•       Coordinate implementation planning with DD&T, R&D, Global Evidence Generation, RWD CoE, and affected business users

•       Capture current-state assessment findings, business requirements, backlog inputs, readiness needs, and unresolved dependencies

•       Track implementation progress, open items, testing outcomes, decisions, support fixes, and ad hoc data retrieval needs

•       Testing, Readiness & Change Support

•       Support user acceptance testing, feedback collection, issue tracking, and readiness validation for approved systems changes

•       Coordinate communications on system changes, enhancements, release impacts, training needs, and transition requirements

•       Maintain handoff materials, implementation notes, decision logs, and future upgrade inputs

•       Support updates related to systems such as the Research Module in iEnvision or equivalent Evidence Generation study platforms

•       Governance, Documentation & Escalation

•       Ensure roadmap documentation is version-controlled, traceable, and linked to relevant system, process, and user-impact records

•       Escalate strategy, design, architecture, prioritization, unresolved dependency, or business-impact questions to Global Evidence Generation, DD&T, or R&D owners

•       Identify duplicative requests, unclear backlog ownership, and process gaps that may affect systems implementation quality

•       Support continuous improvement of systems implementation templates, readiness checklists, and communication materials

•        

Qualifications:

Experience: >2 years of related work experience; >2 years of experience in the biopharmaceutical industry; experience in systems implementation, study systems operations, clinical operations technology, evidence generation operations, project coordination, or medical affairs operations preferred

Technical skills:

•       Working knowledge of study execution systems, evidence repositories, data management platforms, or document / contracting systems

•       Ability to translate approved roadmap initiatives into milestones, dependencies, actions, and implementation trackers

•       Familiarity with UAT, release readiness, backlog management, change communication, issue logs, and transition documentation

•       Strong coordination skills across DD&T, R&D, Global Evidence Generation, RWD CoE, and business users

•       Familiarity with iEnvision Research Module, Veeva, eTMF, CTMS, or similar platforms preferred

Education: A scientific, medical, life sciences, technology, data science, public health, operations, or health economics degree is required

Languages: Fluent English required; additional languages advantageous

Locations

IND - Bengaluru

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time
Source details

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Location & working pattern

IND - Bengaluru

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