Central Monitor – Data Surveillance Lead

About the role

The Central Monitor leads data surveillance activities to support risk‑based monitoring of clinical trials. This role works closely with cross‑functional teams to identify, assess, and mitigate study risks.

Key responsibilities

• Execute centralized monitoring strategies, review trial data, and identify trends, risks, and signals.
• Collaborate with Data Analysts, Risk Surveillance Leads, Study Leaders and other stakeholders to investigate risks and provide recommendations.
• Generate and communicate monitoring findings, document activities, and ensure timely issue resolution.
• Support continuous improvement of monitoring methodologies and ensure compliance with GCP, regulatory requirements and company standards.

Required profile

• University degree in Life Sciences, Business, Operations or related field.
• Minimum 5 years clinical research experience in pharma or CRO, with at least 3 years in monitoring (central or site).
• Strong understanding of RBQM, risk‑based monitoring, KRIs, QTLs and ICH‑GCP.
• Excellent analytical, problem‑solving and stakeholder‑management skills.

Required skills

• Proficiency with clinical data systems.
• Experience using analytics platforms and digital monitoring tools.
• Project management and organizational capabilities.