Sr Manager, Third Party Data Acquisition

Takeda•Boston, MA

22h•$116,000 - $182,270•Onsite

About The Position

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. This role performs TPDA activities at the study and program level, ensuring adherence to applicable study documentation, Takeda quality processes, and regulatory standards. Additionally, the Senior Manager trains and mentors Managers and Coordinators on department processes and standards, supports departmental initiatives, and provides subject matter expertise to support clinical development programs.

Requirements

BS/BA required in health-related, life science, or technology-related fields with minimum 6+ years of drug development experience
Solid understanding of clinical trial processes, documents, ICH-GCP and global regulatory requirements, industry standards, and quality control principles with ability to explain and train others.
Extensive experience managing the acquisition, integration, and oversight of external clinical data from third-party vendors, including vendor relationship management, overseeing delivery, and ensuring data harmonization and validation for seamless integration with Clinical Data Warehouses and analytics platforms.
Excellent project management, organizational, problem-solving, and analytical skills with ability to manage multiple priorities and adapt to changing demands.
Effective communication and collaboration skills across functional groups with proven ability to build relationships in a matrix organization.
Strong mentoring and training capabilities with attention to detail and commitment to quality and compliance.
Advanced proficiency with Microsoft Office applications; experience with TMF systems and clinical data platforms.
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.
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.

Nice To Haves

Stays current with non-EDC clinical data acquisition technologies and supports adoption across studies.

Responsibilities

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.
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.
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.