Senior CDM Leader – Oncology Trials

Merck Healthcare

Warszawa

On-site

PLN 320,000 - 520,000

Full time

5 days ago

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Benefits offered by this job

Health and well-being programs

Career development opportunities

Flexible work options

Job summary

Merck Healthcare in Warsaw leads a complex Clinical Data Management program, overseeing CDM activities across multiple global trials from Phase I to IIIb. The role requires steering data quality, timelines, and cross-functional collaboration in a dynamic matrix structure.

You will manage CROs and vendors, define risk-based data strategies, and ensure compliance with industry standards (CDISC). Leadership across study and program levels is essential, possibly mentoring peers and contributing to

Qualifications

Bachelor's or Master's degree in Life Sciences, Data Management or a related field.
Minimum 10 years of experience in clinical data management in pharma/biotech/healthcare.
Extensive leadership of CDM activities in complex oncology programs and trials.
Strong project management, communication, and problem-solving skills.

Responsibilities

Lead end-to-end clinical data management activities across global trials and programs.
Manage CRO/vendor selection, performance, budgets and timelines.
Define risk-based data collection, cleaning, coding and QA strategies for eCRF and external data.
Mentor colleagues and drive process improvements and SOP development.
Support CDM aspects of regulatory submissions and HA interactions.