Associate Specialist, Pv - Fixed Term Contract, 7 Months

Merck Merck · Pharma · Central District of Israel, Israel

This role supports pharmacovigilance activities within the pharmaceutical industry, focusing on ensuring adherence to regulations, managing adverse event cases, and supporting PV processes. It involves collaboration with internal and external parties, local audits, and maintaining PV procedures.

What you'd actually do

  1. Assists with execution of local PV processes and activities in collaboration with internal functional areas and external parties as assigned. Activities may include but are not limited to management of local PV agreements, local due diligence activities, Post approval Safety Monitoring Program (PSMP) implementation, scheduling and submitting aggregate safety reports.
  2. Assists with day-to-day adverse events case management which may include case intake (where needed), translations (English and/or local language, (as applicable)), acknowledgments, follow-up and submission activities in accordance with PV procedures and country regulations.
  3. Supports local PV audits and inspections when requested.
  4. Participates in issue management/compliance activities and assists in coordinating/preparing the necessary local corrective actions.
  5. Supports development and maintenance of local PV procedures and controlled documents.

Skills

Required

  • Adverse Event Report
  • Adverse Events
  • Compliance Investigations
  • Data Management
  • Drug Safety Surveillance
  • English Language
  • Issue Management
  • Pharmacovigilance
  • Policy Implementation
  • Regulatory Communications
  • Regulatory Compliance Audits

Nice to have

  • Pharmaceutical industry experience
  • General knowledge of AE reporting requirements
  • Health, life science, or medical science degree or equivalent by education/experience
  • Fluent in English (written and spoken)
  • Proficient in local language
  • Good communication, organizational, and time management skills
  • Biological Sciences
  • Business Continuity
  • Data Analysis
  • Data Processing
  • Data Quality Assurance
  • Detail-Oriented
  • Life Science
  • Microbiology
  • Pharmaceutical Management
  • Protocol Development
  • Regulatory Compliance Consulting

What the JD emphasized

  • adherence to all applicable regulations
  • PV regulations
  • local requirements