Pharmacovigilance Activity Manager

ProductLife Group

France

Sur place

EUR 60 000 - 90 000

Plein temps

14 jours+

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Résumé du poste

A leading company in the pharmaceutical manufacturing sector is seeking a Pharmacovigilance Activity Manager with strong experience in compliance and team management. The role involves overseeing a team, engaging with clients, and ensuring accurate safety data management in line with regulatory standards. The ideal candidate will possess a pharmacy degree and several years of relevant experience, with key responsibilities including training, quality control, and project management.

Qualifications

  • Minimum 5-10 years of experience in pharmacovigilance or service providers.
  • Previous experience in data entry and management preferred (5+ years).
  • Understanding of GVP and regulatory standards related to pharmacovigilance.

Responsabilités

  • Oversee PV team, ensuring compliance with regulatory standards.
  • Train junior team members and manage client projects.
  • Conduct Quality Control/Medical Review and participate in audits.

Connaissances

Team Management
Organization skills
Microsoft Office
Fluent in English
Fluent in French
Rigour
Adaptability
Decision-making
Methodical
Sense of priorities

Formation

Pharmacy graduate

Outils

PV databases (e.g., Argus, ArisG)
Microsoft Office

Description du poste

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PLG is looking for a dedicated Pharmacovigilance Activity Manager to join our hub to oversee and work closely with our PV team to ensure compliance with regulatory standards and accurate safety data.

Responsibilities

  • Key trainer for junior team members to increase quality and expand knowledge of PV case processing
  • Review and identify areas of improvement
  • Provide expertise and act as SME for the team, ensuring understanding of tasks by case management team
  • Manage larger client projects and act as single point of contact for the client
  • Monitor client KPI
  • Support in the resolution of NC/CAPA, identify RCA and implement improvements
  • Perform Quality Control/Medical Review and provide support to the team where necessary to ensure regulatory compliance
  • Participate in audits and inspections as required
  • Ensure understanding of client needs and ensure expectations are met and exceeded
  • Organise team meetings as requested

Education and Experience

  • Education: Pharmacy graduate
  • Minimum 5-10 years experience working for service providers
  • Previous experience in data entry, management, or pharmacovigilance (preferably 5+ years).
  • Technical Skills: Proficiency in Microsoft Office and familiarity with PV databases (e.g., Argus, ArisG).
  • Previous experience working to deadlines
  • Knowledge: Understanding of GVP and regulatory standards related to pharmacovigilance.

Skills

  • Sense of priorities
  • Team Management
  • Organization skills
  • Team Spirit
  • Methodical
  • Communicant
  • Ability to make decisions
  • Rigour
  • Adaptability
  • Microsoft office
  • Fluent in both English and French (Oral and Written)

Seniority level
  • Seniority level
    Mid-Senior level
Employment type
  • Employment type
    Full-time
Job function
  • Job function
    Management and Manufacturing
  • Industries
    Pharmaceutical Manufacturing

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