Senior Clinical Data Management Lead for Global Trials

Takeda

Łódź

On-site

PLN 313,000 - 431,000

Full time

14 days+

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Job summary

Takeda in Lodz, Poland is seeking a Senior Manager Clinical Data Management to provide leadership on data management deliverables across studies, ensuring high quality and compliance with ICH‑GCP. You will mentor staff, oversee vendor partnerships, and drive data reviews and CDISC standards adoption to support regulatory submissions.

This role requires strategic mindset, strong project management, and cross‑functional collaboration with global teams. Local travel may be required.

Qualifications

BS/BA in health-related, life science or technology field.
6+ years data management/drug development experience with cross-functional interfaces.
Strong knowledge of FDA/ICH regulations and data management practices.

Responsibilities

Lead data management activities for in-house and outsourced studies; may manage staff.
Oversee vendor oversight across global development programs.
Represent data management on Clinical Sub-team for CRO/Takeda alignment.
Drive data reviews and ensure on-time deliverables with high quality.
Partner with stakeholders and CROs to mitigate risks.
Prepare function for submission readiness and support inspections.