Central Data Monitoring Specialist

vacancy global pro; India; On-site; INR 900,000 - 1,300,000; Full time

Job summary

Priovant is seeking a Central Data Monitoring Specialist to oversee data quality across clinical studies. The role partners with Clinical Operations, CRAs, and Data Management to identify data issues, generate actionable metrics, and ensure data cleaning is completed prior to and during on-site monitoring visits.

The role reports to the Director, Data Management and focuses on real-time remote support to optimize site visit productivity and maintain regulatory compliance.

Qualifications

• Experience in centralized review of study data to identify high-risk data trends, outliers, missing critical data, and potential protocol deviations.
• Ability to generate site-level data quality metrics and dashboards to support monitoring prioritization.
• Experience partnering with Data Management to escalate systemic data trends or recurring discrepancies.

Responsibilities

• Perform ongoing centralized review of study data to identify high-risk data trends, outliers, missing critical 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 endpoint data, SAEs, key 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.
• Provide structured pre-visit briefings to CRAs as needed.

Skills

Data quality monitoring

Clinical data review

CRAs liaison

Data management collaboration

Job description

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

The reputed company provides real-time remote support to optimize site visit productivity, ensure data integrity, and maintain regulatory 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 critical 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 endpoint data, SAEs, key 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.
• Provide structured pre-visit briefings to CRAs as needed.