Your Mission

As a Case Specialist, you will provide specialized pharmacovigilance support, focusing on the review, assessment, and quality control of safety reports. You will play a key role in ensuring compliance with regulatory standards and supporting the team with expert-level case handling.

Group 10
Responsibilities

  • Perform QC for post-marketing cases
  • Analyze ICSR download inclusion/exclusion
  • Review and assess safety reports
  • Query and resolve case discrepancies
  • Ensure compliance with GVP, GCP, FDA, and other regulatory requirements

Group 12
Experience

  • Education & Experience
    • Degree in Pharmacy
    • Minimum 3 years of experience in pharmacovigilance, preferably in a service provider setting
    • Experience with the SafetyEasy database
    • Proven ability to meet deadlines and manage client communications

     

    Languages

    • Fluent in French (required)
    • English (assumed as working language)

     

    Technical Skills

    • Proficiency in Microsoft Office
    • Strong understanding of pharmacovigilance principles and regulatory frameworks
    • Experience with pharmacovigilance databases and QC processes

     

    Bonus Points

    • Strong communication and analytical skills
    • Emotional intelligence and adaptability
    • Reliable, punctual, and well-organized
    • Experience working in multicultural teams

Case Specialist - VAF377

Apply