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Senior Manager, Clinical Data Ingestion

Job in Cambridge, Middlesex County, Massachusetts, 02141, USA
Listing for: Takeda Pharmaceuticals
Full Time position
Listed on 2026-07-01
Job specializations:
  • IT/Tech
    Data Analyst, Data Engineering, Data Security, Data Scientist
Job Description & How to Apply Below

Senior Manager, Clinical Data Configuration

Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Senior Manager, Clinical Data Configuration in our Cambridge, MA office.

At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.

Here, you will be a vital contributor to our inspiring, bold mission.

Objectives:

The Senior Manager, Clinical Data Configuration Representative sits within R&D's Testing, Innovation, and Data Enablement organization and is responsible for configuring study-level clinical data extractions visualizations and transformations across multiple data sources in alignment with Data Transfer Agreements and technical specifications. This role partners with internal and external stakeholders and data engineers to define requirements, resolve issues, and deliver high-quality, compliant data to timelines, while contributing to standards/SOPs, leading process improvements, and mentoring team members to ensure consistent, inspection-ready delivery.

Accountabilities:

  • Configure study-level data extraction and transformations across multiple data sources per Data Transfer Agreement and technical specifications.
  • Partner with internal/external stakeholders and data engineers to define requirements, resolve issues, and deliver to timelines in a matrix environment.
  • Ensure high-quality, compliant data delivery (correct formats/frequency), with readiness to support and defend work in audits/inspections (FDA expectations).
  • Contribute to standards, SOPs, and best practices by providing input, supporting development/maintenance, and participating in related training.
  • Lead process improvement/work streams to improve efficiency and consistency of transfer-spec and configuration execution.
  • Mentor and train team members; provide guidance and knowledge-sharing across the team.
  • Perform quality oversight including review of vendor-performed activities as needed.
  • May mentor/manage Functional Service Providers (FSP)

Education, Behavioral Competencies and

Skills:

Education & Experience

  • Bachelor's degree (e.g., CS, statistics/biostatistics, math, biology/health-related) plus minimum 7 years relevant experience (or equivalent).
  • Experience with EDC build/data management or EDC extraction/configuration; strong understanding of clinical data flow (CDMS, vendor devices, CDR).
  • Familiarity with data cleaning tools (e.g. Veeva CDB, J Review, Elluminate)
  • Strong clinical trial terminology and data transfer specification knowledge; understanding of SDTM.
  • Visualization/configuration: experience designing visual objects and libraries; programming clinical trial visualization tools
  • Data/Integration: XML/standards repositories, APIs, MDR (preferred); ETL/ELT experience; familiarity with AWS/Databricks.
  • Programming (preferred):
    One or more SQL, SAS, R or Python; R Shiny/Python app development.
  • Tools/Ways of Working:
    Microsoft Office
  • Strong project management skills including:
    Initiative, deadline management, strong attention to detail, organization, time management; quick learner comfortable with new tech/systems; able to prioritize competing demands in a fast-paced environment
  • Demonstrated ability to lead projects/work groups
  • Demonstrated ability to resolve issues independently and collaboratively; takes initiative; delivers to deadlines.
  • Prior experience working effectively in a matrix environment; experience mentoring/training others.

This position is currently classified as "hybrid" in accordance with Takeda's Hybrid and Remote Work policy.

Empowering Our People to Shine

Discover more at

No Phone Calls or Recruiters Please.

Takeda Compensation and Benefits Summary

We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.

For

Location:

USA - MA
- Virtual

U.S. Base Salary Range:

$ - $

The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.

The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location.

U.S. based employees may be…

Position Requirements
10+ Years work experience
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