Senior Associate Director, Clinical Data Management

Takeda; Warszawa; On-site; PLN 402,000 - 553,000; Full time

Job summary

Takeda in Warsaw, Poland seeks an Associate Director, Clinical Data Management to lead high-quality CDM deliverables for global programs. The role oversees CDM activities with CROs and vendors, ensures compliance with ICH-GCP, and champions data management excellence across TAUs and departments.

Strong leadership, vendor management, and project oversight are essential, including resource planning, budget management, and readiness for inspections and regulatory submissions.

Qualifications

• 10+ years clinical data management and/or drug development experience.
• Experience managing vendor relationships and alliances.
• Minimum 3 years of line management experience or equivalent.

Responsibilities

• Provide line management and mentoring to CDM staff on projects.
• Oversee CDM activities for studies and programs with internal and external partners.
• Manage external CDM budgets and resource coordination.
• Ensure data collection tools and databases are accurate and inspection-ready.
• Support regulatory submissions and governance with CDM stakeholders.

Skills

Line management

Vendor management

Project management

Data management

Regulatory knowledge

Cross-functional collaboration

Tools

EDC

CDMS

Job description

Takeda in Warsaw, Poland seeks an Associate Director, Clinical Data Management to lead high-quality CDM deliverables for global programs. The role oversees CDM activities with CROs and vendors, ensures compliance with ICH-GCP, and champions data management excellence across TAUs and departments.

Strong leadership, vendor management, and project oversight are essential, including resource planning, budget management, and readiness for inspections and regulatory submissions.