Associate Director, Clinical Data Management – Global Lead

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

Job summary

Takeda in Warsaw, Poland is seeking an Associate Director, Clinical Data Management to lead the delivery of CDM activities across studies, programs and portfolios, including oversight of CROs and external vendors. You will drive leadership, process excellence, and regulatory readiness while coordinating data tools and study data quality with TAUs and cross-functional teams.

This role requires extensive CDM experience, strong vendor management, and proven program management skills in a global

Qualifications

• 10+ years in clinical data management or drug development
• Experience managing vendor relationships for at least 4 years
• 3+ years of line management experience
• Experience supervising staff augmentation (FSP)
• Strong project management and PM skills
• FDA and ICH regulations knowledge

Responsibilities

• Provide line management and mentoring to CDM staff
• Oversee CDM activities for studies with Takeda or CROs
• Ensure timely delivery of CDM deliverables and milestones
• Manage external CDM budgets
• Maintain data tools and data management standards
• Ensure inspection readiness and regulatory readiness

Skills

CDM expertise

Vendor management

Line management

Project management

Regulatory submissions

Cross-functional coordination

Job description

Takeda in Warsaw, Poland is seeking an Associate Director, Clinical Data Management to lead the delivery of CDM activities across studies, programs and portfolios, including oversight of CROs and external vendors. You will drive leadership, process excellence, and regulatory readiness while coordinating data tools and study data quality with TAUs and cross-functional teams.

This role requires extensive CDM experience, strong vendor management, and proven program management skills in a global