Associate Director, CDM — Strategy & Delivery

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

Job summary

Takeda Lodz, Poland is seeking an Associate Director, Clinical Data Management to lead CDM deliverables for global development programs and oversee work with vendors and CRO partners. The role emphasizes strong leadership, regulatory awareness, and process excellence across TAUs, ensuring timely and compliant data management throughout clinical trials.

The AD, CDM champions CDM tools adoption, coordinates external resources, and maintains data tools, databases, and protocols to support

Qualifications

• Minimum 3 years of line management experience or equivalent.
• Proven track record in managing vendor relationships (CROs/FSPs).
• Strong project management skills across large drug development programs.
• Expert knowledge of data management best practices and standards.
• Strategic knowledge of FDA/ICH regulations as they relate to data capture.

Responsibilities

• Direct line management and mentoring of CDM staff.
• Oversee and ensure on-time delivery of CDM deliverables and study data management activities.
• Coordinate with Study Execution Teams and cross-functional partners.
• Manage external CDM budgets and resource allocation.
• Ensure inspection readiness of CDM documents and data management TMF.

Skills

Project management

Vendor management

Team leadership

CDM knowledge

Regulatory knowledge

Job description

Takeda Lodz, Poland is seeking an Associate Director, Clinical Data Management to lead CDM deliverables for global development programs and oversee work with vendors and CRO partners. The role emphasizes strong leadership, regulatory awareness, and process excellence across TAUs, ensuring timely and compliant data management throughout clinical trials.

The AD, CDM champions CDM tools adoption, coordinates external resources, and maintains data tools, databases, and protocols to support