Central Data Monitoring Specialist

Priovant

United States
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Centralized review of study data
Generate site-level data quality metrics
Identify protocol deviations and outliers
** Priovant is seeking a Central Data Monitoring Specialist to oversee data quality in clinical studies, collaborating with various teams to ensure data integrity and regulatory compliance. The role involves real-time support and proactive issue identification to enhance site visit productivity. **

Job Summary

  • The role supports monitoring and site data quality oversight activities across clinical studies focused on autoimmune diseases.
  • The specialist partners closely with Clinical Operations, Clinical Research Associates, and Data Management to identify key data issues.
  • Responsibilities include generating actionable metrics, ensuring critical data cleaning, and providing real-time remote support to optimize site visit productivity.

Matching Summary

Match Score: 75

** Priovant is seeking a Central Data Monitoring Specialist to oversee data quality in clinical studies, collaborating with various teams to ensure data integrity and regulatory compliance. The role involves real-time support and proactive issue identification to enhance site visit productivity. **

Skills & Requirements

Must-have

  • Centralized review of study data
  • Generate site-level data quality metrics
  • Identify protocol deviations and outliers
  • Monitor EDC system data changes
  • Coordinate with Data Management teams

Nice-to-have

  • Experience in autoimmune disease therapies
  • Strong analytical and problem-solving skills
  • Ability to work remotely and collaboratively

Key Requirements

  • Report to Director, Data Management
  • Experience with EDC systems
  • Knowledge of regulatory compliance standards

Work Rights

Not specified

Tailored Resume

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