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As part of the Clinical Data Sciences (CDS) group, an integral delivery unit within the Clinical Development & Operations (CD&O) organization, the Manager, Central Monitor (CM), Data Surveillance is responsible for timely and high quality risk-based monitoring analytics supporting the Pfizer portfolio. The Manager, Central Monitor, Risk Based Monitoring, CDS 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.
Job Responsibility:
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 & methods to ensure customer satisfaction and enable improvements to be implemented during the course of a study
Able to resolve conflicts, influence and communicate cross-functionally with key stakeholders and customers
Set up and test RBM system at study level to ensure system quality
Define key risk indicators (KRIs) in study system, and ensure consistency between the standard level and the study level
Ensure RBM system alignment with the protocol and adherence to ICH GCP, SOPs, corporate standards and regulatory requirements
Work with Study Team to define the issue resolution for the review of findings as signals and actions
Develop, implement and maintain Quality Control related documentation for RBM related activities to ensure data completeness and accuracy
Perform central monitoring activities including review system outputs, propose suggestions for signal and action management, and follow up with study team for the action resolutions
Work with Clinical Data Scientist (CDS) to ensure all signals and actions are properly mitigated and RBM systems properly released
Interact with Clinical Data Scientist (CDS) at study level for deliverables
Interact with other study team members at study level for deliverables
Requirements:
Bachelor’s degree or above in a scientific or business related discipline required
Technical expertise and business experience in supporting clinical trials database development, data management, site monitoring, etc.
Thorough understanding of the processes associated with clinical study management, data management, and regulatory operations
Project management skills and technical capabilities as well as effective verbal and written communication skills in relating to colleagues and associates both inside and outside the organization
Works independently, receives instruction primarily on unusual situations
Ability to organize tasks, time and priorities
ability to multi-task
Ability to communicate effectively and appropriately with internal & external stakeholders, locally and globally
Nice to have:
Working knowledge of clinical development process, understanding concepts of Phase I-IV and principles of study design
Previous experience within a data management role, understanding key processes and principles associated with role including CRF design, database set-up, edit check specification, DMPs and data cleaning activities
Knowledge of clinical trial database and its applications
Knowledge of Windows Environment and its applications (Word, Excel, PowerPoint, Project, etc.)
Experience in Oracle, PL/SQL, SAS, Java, relational database design and database programming skills