Manager, Evidence Generation RWD Lead

IND - 2028 Takeda Innovations India Private Limited

Bengaluru

On-site

INR 900,000 - 1,300,000

Full time

3 days ago
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Job summary

IND - Bengaluru-based Takeda Innovations India Private Limited seeks a Data Ingestion Coordinator to bridge Global Evidence Generation with DD&T ingestion teams. You will manage ingestion requests, perform quality and conformance checks, and track progress with data owners.

The role requires at least 2 years in RWD/data operations, familiarity with OMOP/CDISC, and strong collaboration across DD&T and analytics teams. Fluency in English is required.

Qualifications

  • 2+ years in biopharmaceutical / RWD operations or related data roles.
  • Experience with data quality, conformance checks, and data ingestion processes.

Responsibilities

  • Coordinate ingestion requests and confirm business use case, timing, access, and analytics needs.
  • Apply data quality and conformance checks, document gaps and potential downstream impact.
  • Escalate blockers and coordinate with data owners to resolve issues and improve templates.

Skills

SQL
Data profiling tools
Dashboards
Data catalogs
Quality trackers
RWD operations

Education

Degree in life sciences or related field

Tools

OMOP/CDISC knowledge
SQL

Job description

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: Coordinate RWD data ingestion and quality support, acting as the operational bridge between Global Evidence Generation / RWD CoE business users and DD&T technical ingestion teams. Ensure ingestion requests, data quality checks, conformance checks, trend checks, issue logs, and archival records are complete and traceable to enable DD&T and Global Evidence Generation / RWD owners with fit-for-purpose interpretation and data-readiness decisions.

Key Responsibilities:
Data Ingestion Coordination:
  • Receive requests to ingest new data sources or refresh existing datasets and confirm business use case, source details, required timing, access needs, and intended analytics use
  • Route ingestion requests to DD&T with required intake information, mapping specifications, pipeline requirements, governance constraints, and privacy considerations
  • Track DD&T ingestion progress, dependencies, open questions, clarifications, issue status, and readiness milestones
  • Update data ingestion trackers and store request records, source details, business context, and completion status
Data Quality, Conformance & Trend Checks:
  • Receive datasets or refreshed extracts for quality review with expected use case, quality-check scope, and known data concerns
  • Apply defined data quality, conformance, and trend-check procedures using approved templates and thresholds
  • Run routine checks for completeness, consistency, outliers, expected trends, conformance to standards, and recurring anomalies
  • Document findings, gaps, anomalies, recurring issues, and potential downstream impact
Issue Management & Escalation:
  • Flag unclear gaps, quality concerns, access constraints, or fit-for-purpose questions to US data / evidence owners
  • Coordinate with DD&T and US owners to resolve ingestion blockers, missing inputs, mapping questions, and data quality issues
  • Store check results, issue history, data quality logs, and decision outcomes
  • Support improvements to data quality templates, ingestion trackers, conformance checks, and escalation rules
Qualifications:
Experience:
  • >2 years of related work experience; >2 years of experience in the biopharmaceutical industry; experience in RWD operations, data quality, data management, clinical data operations, HEOR / RWE analytics, or evidence generation operations preferred
Technical skills:
  • Working knowledge of RWD sources, data ingestion workflows, data quality checks, conformance checks, and data issue documentation
  • Familiarity with claims, EHR, registry, trial, or observational datasets
  • Understanding of data standards such as OMOP, CDISC, or equivalent conformance frameworks preferred
  • Ability to coordinate effectively with DD&T, Global Evidence Generation, RWD CoE, data owners, and analytics users
  • Experience with SQL, data profiling tools, dashboards, data catalogs, or quality trackers preferred
Education:
  • A degree in life sciences, public health, epidemiology, data science, biostatistics, pharmacy, medicine, or health economics is required
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. For applicants of U.S and Puerto Rico positions: Click here to learn about our commitment to Equal Employment Opportunity (EEO). If you are limited in the ability to use our job application tool, or otherwise require a reasonable accommodation for a disability please click here.

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