Job Description
Job Title : Pharmacovigilance Specialist
Location : Lawrenceville, NJ
Hours/Schedule: Hybrid 50% onsite
Type: Contract
Responsibilities - 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
- 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
Requirements - 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)
- Strong PowerPoint, Word, and Excel Skills
- Knowledge of Validation processes and associated documentation.
- Excellent verbal, writing, presentation, and project management skills
Benefits System One offers eligible employees health and welfare benefits coverage options, including medical, dental, vision, spending accounts, life insurance, voluntary plans, and participation in a 401(k) plan.
Job Tags
Contract work,