C08 - MEDICAL AND REGULATORY AFFAIRS / PHARMACOVIG - PHARMACOVIGILANCE SPECIALIST - TechDigital
Lawrenceville, NJ
About the Job
Position is Onsite (Lawrenceville/New Brunswick)
Pharmacovigilance (PV) Analytics and Reporting Specialist, PV Analytics Center of Excellence JD
The Pharmacovigilance (PV) Analytics and Reporting Specialist, PV Analytics Center of Excellence is responsible for successful execution, and close-out of activities aligned with the overall vision, strategy, and objectives of the Global Biostatistics & Data Sciences Function. The PV Analytics and Reporting Specialist, PV Analytics Center of Excellence contributes to the ongoing development, implementation, and successful execution of the scientific, operational, and regulatory reporting efforts in line with the overall WWPS needs. The PV Analytics and Reporting Specialist reports to the Senior Manager, PV Analytics Center of Excellence, within Global Biostatistics & Data Sciences. The PV Analytics and Reporting Specialist, PV Analytics Center of Excellence applies a combination of life sciences strategy, leadership, and reporting/visualization experience to drive successful servicing of information needs across WWPS.
Responsibilities include, but are not limited to the following:
Data Analytics and Reporting
Build and continuously improve data analytics through supporting models that provide insights into efficiency, quality, stakeholder feedback, and key performance indicators to drive timely and informed decision making
Maintain and develop reporting databases and analytics applications in environments such as Excel, Tableau, Spotfire, Power BI, SAP Business Objects and/or other Client environments
Leverage internal data systems and tools to efficiently maintain data and reporting processes to minimize manual data retrieving
Liaison with validation team to create validation test script, validation plan, validation summary report and test scripts.
Contribute to qualitative and quantitative research projects through collaboration with data trends from cross-functional teams (Pharmacovigilance, Epidemiology, etc.)
Utilize data analysis tools to aggregate and analyze data to make actional recommendations and answer key business questions
Run and maintain reports regarding activities, outcomes, and be prepared to deliver presentations to management team on a regular and ad-hoc basis
Collect data for monthly reports and quarterly reviews regarding activities, outcomes, and trends of the Advisor team
Continually remain apprised of the constantly changing landscape of the healthcare industry and any impacts it may have to our Analytical programs and reporting mechanisms
Analyze key stakeholder complaints, address rapidly, and discuss with applicable functional leads to collaborate and propose impactful and realistic solutions
Maintain data integrity and traceability across the transformation lifecycle from the Source to Target
Support program and project team activities required to implement innovation initiatives.
Contribute to the management and prioritization of process improvement and innovation initiatives
Define and provide metric reporting and data analysis for GBDS/WWPS initiatives including relevant insights to facilitate decision-making process
Assess and interpret the process impact of new PV tools and processes
Skills/Knowledge Required:
Life Sciences, Information, or similar background (Bachelors, Masters)
5+ years Drug Safety/Pharmacovigilance experience
Advanced Tableau, Spotfire, Power BI, SAP Business Objects (BO) skills with 5+ years of development experience
Databases (Postgres, Oracle, MS Access, Impala, SharePoint List etc.)
Programming languages (SQL, VBA, Python etc.)
Reporting platforms and services (Cognos, SAP-Business Objects, Power BI etc.)
Knowledge and application of commercial coding dictionaries (MedDRA, WHO Drug)
Ability to organize/curate data and see big picture from scattered pieces of information
Knowledge of taxonomies, ontologies, and other knowledge management constructs
Analytical and strategic thinking skills required
Strong PowerPoint, Word, and Excel Skills
Knowledge of Validation processes and associated documentation.
Excellent verbal, writing, presentation, and project management skills
Strong strategic orientation with ability to translate into operational priorities and plans
Ability to promote cooperation and commitment within a team to achieve goals and deliverables.
Ability to resolve complex problems and manage difficult stakeholder situations
Ability to lead the development of critical path analyses and support scenario planning
Promotes and practices effective pro-active decision-making, ensuring timely coordination and dissemination of information
Demonstrated ability to work on multiple projects
Strong willingness to collaborate with cross-functional partners
Flexible, team member with positive attitude, friendly demeanor, ability to prioritize projects and balance competing priorities
Confidentiality and integrity are required
Pharmacovigilance (PV) Analytics and Reporting Specialist, PV Analytics Center of Excellence JD
The Pharmacovigilance (PV) Analytics and Reporting Specialist, PV Analytics Center of Excellence is responsible for successful execution, and close-out of activities aligned with the overall vision, strategy, and objectives of the Global Biostatistics & Data Sciences Function. The PV Analytics and Reporting Specialist, PV Analytics Center of Excellence contributes to the ongoing development, implementation, and successful execution of the scientific, operational, and regulatory reporting efforts in line with the overall WWPS needs. The PV Analytics and Reporting Specialist reports to the Senior Manager, PV Analytics Center of Excellence, within Global Biostatistics & Data Sciences. The PV Analytics and Reporting Specialist, PV Analytics Center of Excellence applies a combination of life sciences strategy, leadership, and reporting/visualization experience to drive successful servicing of information needs across WWPS.
Responsibilities include, but are not limited to the following:
Data Analytics and Reporting
Build and continuously improve data analytics through supporting models that provide insights into efficiency, quality, stakeholder feedback, and key performance indicators to drive timely and informed decision making
Maintain and develop reporting databases and analytics applications in environments such as Excel, Tableau, Spotfire, Power BI, SAP Business Objects and/or other Client environments
Leverage internal data systems and tools to efficiently maintain data and reporting processes to minimize manual data retrieving
Liaison with validation team to create validation test script, validation plan, validation summary report and test scripts.
Contribute to qualitative and quantitative research projects through collaboration with data trends from cross-functional teams (Pharmacovigilance, Epidemiology, etc.)
Utilize data analysis tools to aggregate and analyze data to make actional recommendations and answer key business questions
Run and maintain reports regarding activities, outcomes, and be prepared to deliver presentations to management team on a regular and ad-hoc basis
Collect data for monthly reports and quarterly reviews regarding activities, outcomes, and trends of the Advisor team
Continually remain apprised of the constantly changing landscape of the healthcare industry and any impacts it may have to our Analytical programs and reporting mechanisms
Analyze key stakeholder complaints, address rapidly, and discuss with applicable functional leads to collaborate and propose impactful and realistic solutions
Maintain data integrity and traceability across the transformation lifecycle from the Source to Target
Support program and project team activities required to implement innovation initiatives.
Contribute to the management and prioritization of process improvement and innovation initiatives
Define and provide metric reporting and data analysis for GBDS/WWPS initiatives including relevant insights to facilitate decision-making process
Assess and interpret the process impact of new PV tools and processes
Skills/Knowledge Required:
Life Sciences, Information, or similar background (Bachelors, Masters)
5+ years Drug Safety/Pharmacovigilance experience
Advanced Tableau, Spotfire, Power BI, SAP Business Objects (BO) skills with 5+ years of development experience
Databases (Postgres, Oracle, MS Access, Impala, SharePoint List etc.)
Programming languages (SQL, VBA, Python etc.)
Reporting platforms and services (Cognos, SAP-Business Objects, Power BI etc.)
Knowledge and application of commercial coding dictionaries (MedDRA, WHO Drug)
Ability to organize/curate data and see big picture from scattered pieces of information
Knowledge of taxonomies, ontologies, and other knowledge management constructs
Analytical and strategic thinking skills required
Strong PowerPoint, Word, and Excel Skills
Knowledge of Validation processes and associated documentation.
Excellent verbal, writing, presentation, and project management skills
Strong strategic orientation with ability to translate into operational priorities and plans
Ability to promote cooperation and commitment within a team to achieve goals and deliverables.
Ability to resolve complex problems and manage difficult stakeholder situations
Ability to lead the development of critical path analyses and support scenario planning
Promotes and practices effective pro-active decision-making, ensuring timely coordination and dissemination of information
Demonstrated ability to work on multiple projects
Strong willingness to collaborate with cross-functional partners
Flexible, team member with positive attitude, friendly demeanor, ability to prioritize projects and balance competing priorities
Confidentiality and integrity are required
Source : TechDigital
