Pharmacovigilance Data Analyst

4 weeks ago

Trenton, New Jersey, United States Axelon Full time
Job Title: Pharmacovigilance Specialist

Job Summary:

The Pharmacovigilance Specialist will be responsible for the successful execution and close-out of activities aligned with the overall vision, strategy, and objectives of the Global Biostatistics & Data Sciences Function.

Key Responsibilities:

  • Develop and maintain data analytics models to provide insights into efficiency, quality, stakeholder feedback, and key performance indicators.
  • 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.
  • Collaborate with cross-functional teams to contribute to qualitative and quantitative research projects.
  • Utilize data analysis tools to aggregate and analyze data to make actionable 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)
  • 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 proactive 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

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