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Pharmacovigilance (PV) Analytics and Reporting Specialist

Pharmacovigilance (PV) Analytics and Reporting Specialist

Reference: BBBH28600
Date posted: 17/03/2026
Job details
Specialism
PVG & Drug Safety
Expertise
Global Drug Safety
Location
Lawrence Township, New Jersey, USA
Job type
Contract
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Description

Where pharmacovigilance meets analytics-transform data into decisions that protect patients worldwide.

R&D Partners is seeking a Pharmacovigilance (PV) Analytics and Reporting Specialist to join a leading pharmaceutical company. This role focuses on supporting the PV Analytics Center of Excellence in delivering scientific, operational, and regulatory reporting aligned with global biostatistics and data sciences objectives. The ideal candidate will leverage their expertise in data analytics, reporting tools, and pharmacovigilance processes to drive informed decision-making and process improvements.

Applicants must have legal authorization to work in the United States.

Responsibilities:

Data Analytics and Reporting:

  • Develop and enhance data analytics models to provide insights into efficiency, quality, stakeholder feedback, and KPIs.
  • Maintain and develop reporting databases and applications using tools like Excel, Tableau, Power BI, SAP Business Objects, etc.
  • Minimize manual data retrieval by leveraging internal systems and tools.

Validation and Compliance:

  • Collaborate with validation teams to create test scripts, validation plans, and summary reports.
  • Ensure data integrity and traceability across the transformation lifecycle.

Process Improvement:

  • Support program and project activities to implement innovation initiatives.
  • Define and report metrics for GBDS-PS initiatives to facilitate decision-making.

Key Skills and Requirements:

  • Education: Bachelor’s degree required.
  • Industry Experience: Pharma/biotech industry experience essential.

Technical Expertise:

  • Advanced proficiency in SAP Business Objects (v4.3), Tableau, Power BI, and SQL.
  • Experience with Spotfire preferred.
  • Strong skills in PowerPoint, Word, and Excel.
  • Pharmacovigilance Knowledge: Drug safety experience required.
  • Analytical Skills: Ability to organize and curate data, analyze trends, and see the big picture.
  • Validation Knowledge: Familiarity with validation processes and documentation.

Soft Skills:

  • Strategic thinking and problem-solving abilities.
  • Excellent communication, presentation, and project management skills.
  • Collaborative mindset with flexibility to balance competing priorities.
  • Integrity and confidentiality are essential.

For more information, please contact William Tyler.

If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page.

R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you’ve read and understood our privacy policy, which informs you how we process and safeguard your data – https://www.r-dpartners.com/privacy-policy/

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