Central Monitor Senior Associate
Core
Execute proactive, data-driven central monitoring across clinical studies to detect early signals impacting patient safety, data quality, and protocol adherence.
Role type
Senior Central Monitor (Clinical Development)
Builds
Clinical trial data quality and risk mitigation strategies
Domain
Biotechnology / Clinical Trials
Required skills
Central monitoring analytics, risk-based quality management (RBQM), statistical signal detection, stakeholder engagement, mentoring, inspection-ready documentation
Preferred skills
Global clinical trial experience, clinical site management, broad clinical trial data analysis, central monitoring tools expertise
Responsibilities
Execute risk surveillance for assigned studies/sites, perform independent signal detection and triage, support RBQM strategy implementation, conduct study-specific analytics and trend reviews, ensure high-quality documentation of monitoring outputs, mentor junior central monitors
Seniority
Senior, hands-on IC