Senior Central Data Monitor — Risk & Data Quality Lead

Merck Healthcare; Warszawa; Hybrid; PLN 180,000 - 240,000; Full time

Benefits offered by this job

Private medical care

Life insurance

Sports card

Flexible working hours

Job summary

Merck Healthcare is seeking a Senior Central Data Monitor to lead the identification and communication of risk signals in clinical studies. You will collaborate across functions to ensure data integrity and support risk-based quality oversight.

You will analyze data trends, contribute to study plans, and monitor corrective actions, while ensuring compliance with industry regulations and driving continuous improvement.

Qualifications

• Advanced degree in Life Sciences or a related field.
• 7+ years of experience in central data monitoring, with experience in clinical data management, site monitoring, or risk-based quality management.
• Strong knowledge of ICH GCP and regulatory requirements.
• Proficient in data visualization and risk-based monitoring tools (e.g., CluePoints) and MS Office.
• Excellent analytical and problem-solving skills.
• Effective communicator with leadership capabilities.
• Ability to manage multiple projects and priorities.
• Detail-oriented and results-driven mindset.

Responsibilities

• Lead identification and communication of risk signals in clinical studies.
• Collaborate with cross-functional teams to ensure data integrity and support risk-based quality oversight.
• Support development of applicable study plans and analyze data trends.
• Contribute to risk review meetings and monitor corrective actions implementation.
• Oversee quality checks to ensure compliance with industry regulations and drive continuous improvement in central data monitoring processes.

Skills

Central data monitoring

ICH GCP knowledge

Data visualization

Leadership

Education

Advanced degree in Life Sciences

Tools

CluePoints

MS Office

Job description

Merck Healthcare is seeking a Senior Central Data Monitor to lead the identification and communication of risk signals in clinical studies. You will collaborate across functions to ensure data integrity and support risk-based quality oversight.

You will analyze data trends, contribute to study plans, and monitor corrective actions, while ensuring compliance with industry regulations and driving continuous improvement.