Manager, Evidence Generation Data Governance & Systems Lead

Overview

Support implementation of approved Evidence Generation systems roadmap changes with DD&T and R&D, maintaining implementation discipline, decision logs, backlog updates, dependency tracking, and handoff materials.

What you'll do

• 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.
• 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.
• 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.

What you'll need

• More than 2 years of related work experience.
• More than 2 years of experience in the biopharmaceutical industry.
• A scientific, medical, life sciences, technology, data science, public health, operations, or health economics degree.
• Fluent English.
• 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.

Nice to have

• Experience in systems implementation, study systems operations, clinical operations technology, evidence generation operations, project coordination, or medical affairs operations.
• Familiarity with iEnvision Research Module, Veeva, eTMF, CTMS, or similar platforms.
• Additional languages.

Details

• Location: Bengaluru, India.
• Employment type: Full time, Regular employee.