Central Data Monitoring Specialist

Central Data Monitoring Specialist
United States
Remote 

Priovant is committed to developing therapies that address high unmet need in autoimmune disease. The Central Data Monitoring Specialist (CDMS) supports monitoring and site data quality oversight activities across clinical studies. The role partners closely with Clinical Operations, Clinical Research Associates, Data Management, and external vendors to proactively identify key data issues, generate actionable metrics, and ensure critical data cleaning activities prior to and during on-site monitoring visits.

The CDMS provides real-time remote support to optimize site visit productivity, ensure data integrity, and compliance. S/he will report to the Director, Data Management.

Responsibilities
Perform ongoing centralized review of study data to identify high-risk data trends, outliers, missing data, and potential protocol deviations.

Generate site-level data quality metrics and dashboards to support monitoring prioritization.

Identify key priority data requiring cleaning prior to on-site visits (e.g., eligibility criteria, primary endpoints, safety labs).

Partner with Data Management to escalate systemic data trends or recurring discrepancies.

Prepare pre-visit data cleaning summaries and site-specific issue trackers for CRAs.

Highlight unresolved queries, overdue data entry, missing signatures, and critical form status gaps.

Support risk-based monitoring activities and centralized monitoring processes across clinical trials.

Collaborate cross-functionally with Clinical Operations, Biostatistics, Medical Monitoring, and site personnel.

Ensure compliance with Google Cloud Platform, SOPs, and study protocols.

Assist in developing reports, visualizations, and data review tools to improve study oversight.