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Senior Pharmacovigilance Specialist

RemoteNot specified
Published
Role
Fullstack
Experience
Senior
Employment
Full-time
Salary not disclosed
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No BS summary

Senior Pharmacovigilance Specialist is responsible for supporting global and local PV systems and ensuring compliance with all PV activities with international or local regulations. May overtake additional regional or local PV responsible person roles for simple PV systems. The position is remote, home-based in any EU country.

Core skills

PharmacovigilanceCase ProcessingAggregate Safety Reports (ASR) management for GxP PV compliance per EU regulations and company procedures (pre- and post-authorization setting): maintains reports meeting regulatory deadlines and quality standards by synthesis and analysis of safety data trends against historical data and program flags to produce comprehensive safety reports for regulatory submission, accurately evaluates available source data for report completeness, trends outliers, / exceeds action thresholds, outliers, / exceeds specific procurement lead consecutive events and comprehension risks for internal stakeholders and to ensure their accuracy and completeness; communicates critical issues professionally, and escalates transparently and aligns on proposals; without supervisor, makes notes and line lists, reference data rule database references compile roll-outs, routing, date gap identifier NOC-predictable content nom, World Safety Agreement meets business requirements neighboring accommodating and minimizes non-alignment across modalities; identifies protocol risks, scope of audit and closure expected closure across own effectiveness dashboards and; leverages factual PV database comparisons and automations for insights organized at scale.

Required skills

MS OfficePV databases

Required languages

English Fluent

What you'll do

  • Act as the Project Manager or deputy Project Manager for the assigned projects
  • Perform accurate forecasting and contribute to budget planning, ensuring efficient functioning of the QPPV Office
  • Update SOPs and act as a subject matter expert for Pharmacovigilance in assigned company processes
  • Maintain KPI reports and execute core and standard safety activities for assigned contractual partners
  • Manage Full or local Pharmacovigilance systems and projects (or part of them) and/or central pharmacovigilance activities (e.g., end-to-end case processing, Aggregate Safety Reports, Risk Management Plans and risk minimization activities) in both pre- and post-authorization setting (as applicable)
  • Act as a customer contact point (as applicable), ensuring consistent communication and management for assigned projects
  • Act as the appointed EU QPPV or deputy EU QPPV in accordance with a separate QPPV Job Description (if applicable)
  • Ensure high-quality performance of Pharmacovigilance services in assigned region/country and timely communication with Health Authorities
  • Ensure inspection/audit readiness and finding remediation

Benefits

  • Professional growth and career opportunities
  • International team and diverse company culture
  • Annual-time and performance-based bonus
  • Employee and dependents' health insurance (Kenya, Nigeria, and Egypt insurance if eligible)
  • Personal & accident insurance and business trip insurance
  • Additional health insurance
  • Remote/home-based
  • Flexible work arrangements supporting work-life growth (policies such as cell phone, PTO, and flexible working hours
  • Home office equipment provided
  • Team building, global meetings, active events
Pharmaceutical / Biotech
Salary not disclosed