Strategic Lead, Third-Party Data Acquisition

Takeda Pharmaceutical Company Limited; Boston (MA); On-site; USD 116,000 - 182,000; Full time

Job summary

Takeda Pharmaceutical Company Limited in Boston, MA is seeking a Senior Manager, Third-Party Data Acquisition (TPDA) to ensure integrity, compliance, and timely delivery of non-EDC data from external vendors across studies and programs.

You will lead TPDA activities in cross-functional settings, mentor Managers and Coordinators, and drive process improvements while ensuring adherence to ICH-GCP, CDISC SDTM/ADaM, and regulatory standards.

Qualifications

• BS/BA in health-related, life science, or technology-related fields is required.
• Minimum 6+ years of drug development experience.
• Strong understanding of ICH-GCP and global regulatory requirements.
• Experience managing acquisition, integration, and oversight of external clinical data from third-party vendors.
• Ability to train and mentor staff on TPDA processes and standards.

Responsibilities

• Ensure data integrity, compliance, and timely delivery of third-party data across studies and programs.
• Serve as escalation point for study- and program-level issues with cross-functional teams.
• Monitor data deliverables to identify and resolve inconsistencies in process and standards adherence.
• Coach Managers and Coordinators on TPDA processes, standards, and vendor considerations.
• Collaborate with cross-functional stakeholders to drive alignment and process improvements.
• Represent TPDA in meetings and support regulatory inspections and audits.

Skills

Data governance

Project management

Cross-functional collaboration

Mentoring

CDISC/SDTM/ADaM

Communication

Education

BS/BA in health-related, life science, or technology-related fields

Tools

Microsoft Office

TMF systems

Clinical data platforms

Job description

Takeda Pharmaceutical Company Limited in Boston, MA is seeking a Senior Manager, Third-Party Data Acquisition (TPDA) to ensure integrity, compliance, and timely delivery of non-EDC data from external vendors across studies and programs.

You will lead TPDA activities in cross-functional settings, mentor Managers and Coordinators, and drive process improvements while ensuring adherence to ICH-GCP, CDISC SDTM/ADaM, and regulatory standards.