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Sr Manager, Third Party Data Acquisition
Job in
Boston, Suffolk County, Massachusetts, 02298, USA
Listed on 2026-10-15
Listing for:
Takeda
Full Time
position Listed on 2026-10-15
Job specializations:
-
Security
Information Security & Data Protection
Job Description & How to Apply Below
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.
- 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.
- 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.
- 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.
- 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.
- 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.
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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