Manager, Evidence Generation Operations Enablement (non-site based)
Takeda Pharmaceutical Company Limited (company site, opens in a new tab)5+ yrsBengaluruOn-siteDirect career pageEst. 12–20 LPA
Posted 20h ago
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Job description
Structured overview of role & requirements
About This Role
- Manage non-site-based study operations including intake, documentation tracking, close-out processes, Fair Market Value (FMV) support, contracting, and vendor artifact management.
- Coordinate cross-functional review logistics, escalate conflicts to appropriate owners, and maintain audit-ready repositories and trackers for multiple studies.
- Drive process improvements and utilize approved digital, automation, and AI tools to ensure operational accuracy, traceability, and compliance.
Minimum Requirements
- Bachelor's degree in scientific, medical, life sciences, pharmacy, public health, operations, health economics, or related discipline.
- More than 5 years total related work experience with at least 2 years in the biopharmaceutical industry.
- Experience in evidence generation operations, clinical/HEOR/Medical Affairs operations, study coordination, contract administration, or vendor operations.
- Fluent in English; familiarity with tools like iEnvision Research Module or Veeva Vault preferred.
Ideal Candidate Profile
- Experienced in coordinating multidisciplinary teams including Legal, Compliance, Finance, Procurement, and study teams within global evidence generation environments.
- Skilled at managing multiple concurrent operational workstreams with high attention to detail and maintaining audit-ready documentation.
- Comfortable leveraging automation and AI-enabled tools for operational tasks while maintaining compliance and escalation protocols.