Job Details

A company is looking for a Central Data Monitoring Specialist to support monitoring and site data quality oversight activities across clinical studies.Key ResponsibilitiesPerform ongoing centralized review of study data to identify data trends and potential protocol deviationsGenerate site-level data quality metrics and dashboards to support monitoring prioritizationProvide remote data review support and assist with issue resolution during on-site visitsRequired QualificationsBachelor's degree in life sciences or equivalent knowledge and experience2+ years of experience in the biopharmaceutical industry or related fieldProficiency with Medidata RAVE EDC systemExperience in clinical data review and sample managementOrganized and collaborative with a high sense of urgency and drive for results