Central Monitor II

📋 Description Central monitoring of clinical trial data quality and integrity Lead RBQM plan development and risk assessments Collaborate with functions to identify KRIs and monitor data Conduct centralized statistics monitoring and remote data review Prepare reports and sponsor communications Mentor junior colleagues and help develop processes 🎯 Requirements Bachelor’s in life sciences/stats/data/clinical ops or equivalent At least 2 years in clinical monitoring or trial management Working knowledge of ICH GCP and clinical development Excellent communication, organizational and English skills Ability to work independently or in a team and learn data extraction Proficiency in statistical analysis and data monitoring tools 🎁 Benefits Competitive benefits package Opportunities for process improvement and career growth Collaborative, cross-functional team environment