Director, Group Lead, Data Surveillance, Clinical Data Sciences

Pf Health

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Risk-based monitoring analytics
Central monitoring deliverables oversight
Clinical trial monitoring strategy
** Pf Health is seeking a Director, Group Lead for Data Surveillance within its Clinical Data Sciences unit. This leadership role focuses on implementing risk-based monitoring strategies and overseeing central monitoring deliverables to ensure high-quality clinical data for Pfizer's portfolio. **

Job Summary

  • The Director, Group Lead, Data Surveillance is responsible for the delivery of all technical and operational aspects of RBM, including timely and high-quality risk-based monitoring analytics supporting the Pfizer portfolio.
  • The role involves managing Central Monitoring groups, providing oversight of central monitoring deliverables and managerial oversight of Central Monitors.
  • Responsibilities include defining, delivering, and executing the enterprise-level RBM implementation plan, encompassing strategy, process definition, technology implementation, training, change management, and communication.

Matching Summary

Match Score: 75

** Pf Health is seeking a Director, Group Lead for Data Surveillance within its Clinical Data Sciences unit. This leadership role focuses on implementing risk-based monitoring strategies and overseeing central monitoring deliverables to ensure high-quality clinical data for Pfizer's portfolio. **

Skills & Requirements

Must-have

  • Risk-Based Monitoring analytics
  • Central monitoring deliverables oversight
  • Clinical trial monitoring strategy
  • Data collection and assimilation solutions
  • Relational databases and data visualization tools

Nice-to-have

  • Global, matrix environment leadership
  • Programming in clinical trial environment
  • Commercial RBQM systems experience
  • Risk-based monitoring principles knowledge

Key Requirements

  • Bachelor's Degree in Life Sciences, Informatics, Computer Science, Statistics, or related business degree
  • 15+ years relevant experience including team management
  • Master's degree preferred
  • Experience in pharmaceutical, biotech, CRO, or Regulatory Agency
  • Experience managing complex projects
  • Working knowledge of all phases of clinical trials
  • Strong Project and Risk Management skills
  • Understanding of regulatory requirements and data standards

Work Rights

Not specified

Tailored Resume

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