Senior CDM Lead: Data Strategy & Program Oversight

6999 Takeda SCE; Poland; On-site; PLN 313,000 - 431,000; Full time

Job summary

Takeda SCE in Lodz, Poland is seeking a Senior Manager Clinical Data Management to lead data management activities for in-house and outsourced studies. You will oversee vendor partnerships, ensure regulatory alignment, and drive data quality across programs.

The role requires 6+ years in data management, strong CDISC knowledge, and cross-functional leadership to support submissions and inspections. This position is based in Lodz with full-time hours.

Qualifications

• BS/BA required preferably in a health-related, life science area or technology-related fields.
• 6+ years of experience in data management and/or drug development with cross-functional interfaces.
• Proven project management experience and handling data management activities for large programs.
• Knowledge of FDA/ICH regulations and CDISC standards.

Responsibilities

• Lead data management activities for in-house and outsourced studies; may manage staff.
• Oversee vendor activities across global development programs.
• Represent data management in the Clinical Sub-team for data deliverables and submissions.
• Collaborate with Takeda stakeholders to meet milestones and quality.
• Maintain TMF documents and ensure archival and inspection readiness.
• Plan external Data Management budgets and timelines.
• Drive continuous improvement and implementation of tools.

Skills

Data management

Project management

Vendor oversight

CDISC standards

Regulatory knowledge

Cross-functional leadership

Problem solving

Communication

Education

BS/BA in life sciences or tech fields

Tools

CDMS

SAS

SQL

Oracle Clinical

Job description

Takeda SCE in Lodz, Poland is seeking a Senior Manager Clinical Data Management to lead data management activities for in-house and outsourced studies. You will oversee vendor partnerships, ensure regulatory alignment, and drive data quality across programs.

The role requires 6+ years in data management, strong CDISC knowledge, and cross-functional leadership to support submissions and inspections. This position is based in Lodz with full-time hours.