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ROLE SUMMARY

As part of the Clinical Data Sciences group, an integral delivery unit within the Global Biometrics and Data Management (GBDM) organization, the Associate Manager, Central Monitor (CM), Data Surveillance is responsible for timely and high quality risk-based monitoring analytics supporting the Pfizer portfolio with minimum supervision. The Associate Manager, Central Monitor, Data Surveillance will support an approach to clinical trial monitoring which utilizes data and site level information to determine needs for performing on-site, remote and centralized activities and focuses resources on risks that have the most potential to impact patients’ safety and data quality, with supervision.

ROLE RESPONSIBILITIES

General:

• Implement global strategies, initiatives, processes, and standards to ensure consistent, efficient, and quality processes to meet quality, timelines and deliverables.

• Provide technical expertise to set up and test study level Risk-based Monitoring system

• Review study level system outputs to process for the signal and action management

• Plan and execute communication plans