Manager, Operations Enablement
Takeda Pharmaceutical Company Limited (company site, opens in a new tab)BengaluruOn-siteDirect career pageEst. 14–22 LPA
Posted 21h ago
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Job description
Structured overview of role & requirements
About This Role
- Manage and coordinate intake, documentation, review, contracting, and close-out activities for multiple non-site-based studies across Global Evidence Generation and other functional teams.
- Maintain audit-ready documentation, track study progress, FMV records, vendor artifacts, and contractual materials ensuring compliance and traceability.
- Identify process gaps and implement improvements using approved digital, automation, and AI-enabled tools for operational efficiency and reporting.
Minimum Requirements
- Bachelor's degree in scientific, medical, life sciences, pharmacy, public health, operations, health economics, or related discipline.
- More than 5 years of related work experience; at least 2 years in biopharmaceutical industry preferred, including evidence generation operations, clinical or HEOR operations, Medical Affairs, contract administration, or vendor operations.
- Working knowledge of study operations including intake management, documentation tracking, study close-out, cross-functional review coordination, and contracting workflows.
- Location: Bengaluru, India (onsite presence implied); Fluent English required.
Ideal Candidate Profile
- Experienced in coordinating cross-functional teams involving Global Evidence Generation, Legal, Compliance, Finance, Procurement, and vendors supporting multi-study management.
- Skilled in managing audit-ready repositories and complex documentation with high attention to detail and ability to handle multiple concurrent workstreams.
- Comfortable leveraging digital tools and AI-enabled solutions with sound judgment for operational accuracy, privacy, and compliance.