Central Data Monitoring Specialist

Job Summary

A company is looking for a Central Data Monitoring Specialist to support monitoring and site data quality oversight activities across clinical studies.

Key Responsibilities

• Perform ongoing centralized review of study data to identify data trends and potential protocol deviations
• Generate site-level data quality metrics and dashboards to support monitoring prioritization
• Provide remote data review support and assist with issue resolution during on-site visits

Required Qualifications

• Bachelor's degree in life sciences or equivalent knowledge and experience
• 2+ years of experience in the biopharmaceutical industry or related field
• Proficiency with Medidata RAVE EDC system
• Experience in clinical data review and sample management
• Organized and collaborative with a high sense of urgency and drive for results