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Sr Manager, Third Party Data Acquisition

Job in Boston, Suffolk County, Massachusetts, 02298, USA
Listing for: Takeda
Full Time position
Listed on 2026-10-15
Job specializations:
  • Security
    Information Security & Data Protection
Salary/Wage Range or Industry Benchmark: 116000 - 182000 USD Yearly USD 116000.00 182000.00 YEAR
Job Description & How to Apply Below
Job Description OBJECTIVES/

PURPOSE:
  • The Senior Manager, Third-Party Data Acquisition (TPDA) is accountable for ensuring the integrity, compliance, and timely delivery of non-EDC data from third-party vendors throughout the data lifecycle for assigned studies and programs.
  • Performs TPDA activities at the study and program level, ensuring adherence to applicable study documentation, Takeda quality processes, and regulatory standards.
  • Trains and mentors Managers and Coordinators on department processes and standards, supports departmental initiatives, and provides subject matter expertise to support clinical development programs.
ACCOUNTABILITIES :
  • Performs TPDA activities for assigned studies and programs to ensure compliance, quality, and audit readiness.
  • Serves as escalation point for study and program-level issues and collaborates with cross-functional stakeholders to support study objectives.
  • Monitors data deliverables across assigned studies and programs to identify, resolve, and prevent inconsistencies in process and standards adherence.
  • Trains and mentors Managers and Coordinators on TPDA processes, standards, and best practices.
  • Contributes to assigned departmental initiatives focused on process improvements.
Technical Expertise
  • Comprehensive knowledge of end-to-end third-party data integration processes, including validation, operationalization, and ongoing optimization.
  • Experience working effectively in complex matrix environments with cross-functional stakeholders, understanding their roles in data generation, acquisition, ingestion, summarization, and reporting across a large clinical portfolio.
  • Strong understanding of clinical data standards (CDISC, SDTM, ADaM), data governance practices, and diverse data formats and structures across non-EDC technologies, including eCOA, IRT, laboratories, wearables, imaging, and other third-party data sources.
  • Stays current with non-EDC clinical data acquisition technologies and supports adoption across studies.
Leadership
  • Provides hands-on execution of planning, setup, transfer, and acquisition of third-party clinical data across assigned studies and programs, ensuring alignment with study objectives and regulatory requirements.
  • Trains and mentors Managers and Coordinators on TPDA processes, standards, and vendor and study specific considerations.
  • Collaborates effectively with cross-functional stakeholders to drive alignment and informed decision-making, and supports change management for assigned process improvements and departmental initiatives.
Interaction :
  • Performs study and program-level activities, building collaborative relationships with cross-functional teams and external stakeholders within a complex matrix environment.
  • Manages timely delivery of TPDA deliverables across multiple concurrent programs.
  • Engages with external vendors to facilitate alignment on processes, expectations, and issue resolution at the study and program levels.
  • Represents TPDA in study and program team meetings, supports regulatory inspections and audits, and participates in departmental and company-wide initiatives as assigned.
Complexity :
  • Manages multiple concurrent studies with unique data acquisition requirements across various therapeutic areas and development phases.
  • Navigates complex matrix organization with multiple stakeholders and competing demands, coordinating across functional groups while managing resource constraints and vendor capabilities.
  • Works with diverse vendor types and technologies, and adapts to evolving regulatory landscape and pharmaceutical development environment.
EDUCATION, BEHAVIOURAL COMPETENCIES AND

SKILLS:
  • BS/BA required in health-related, life science, or technology-related fields with minimum 6+ years of drug development experience
  • Solid…
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