Activez les alertes d’offres d’emploi par e-mail !

Playworker

JR France

Lyon

Sur place

EUR 50 000 - 70 000

Plein temps

Il y a 8 jours

Mulipliez les invitations à des entretiens

Créez un CV sur mesure et personnalisé en fonction du poste pour multiplier vos chances.

Résumé du poste

A leading company in pharmacovigilance is seeking a dedicated Pharmacovigilance Specialist to oversee compliance and safety data management. The role involves training junior staff, managing client projects, and ensuring regulatory standards are met. Ideal candidates will have significant experience in pharmacovigilance and strong communication skills in both English and French.

Qualifications

  • Minimum 5-10 years' experience working for service providers.
  • Previous experience in data entry, management, or pharmacovigilance (preferably 5+ years).

Responsabilités

  • Serve as the key trainer for junior team members.
  • Review cases and identify areas for improvement.
  • Manage larger client projects and serve as the single point of contact for clients.

Connaissances

Prioritization
Team management
Organization
Team spirit
Methodical approach
Strong communication
Decision-making
Rigour
Adaptability

Formation

Pharmacy graduate

Outils

Microsoft Office
PV databases

Description du poste

Social network you want to login/join with:

PLG is seeking a dedicated Pharmacovigilance Specialist - Case Processing to join our hub. The successful candidate will oversee and collaborate closely with our PV team to ensure compliance with regulatory standards and accurate safety data management.

Responsibilities
  1. Serve as the key trainer for junior team members to enhance quality and expand knowledge in PV case processing.
  2. Review cases and identify areas for improvement.
  3. Provide expertise and act as SME for the team, ensuring clear understanding of tasks by the case management team.
  4. Manage larger client projects and serve as the single point of contact for clients.
  5. Monitor client KPIs.
  6. Support in resolving NC/CAPA, identify RCA, and implement improvements.
  7. Perform Quality Control/Medical Review and support the team to ensure regulatory compliance.
  8. Participate in audits and inspections as required.
  9. Ensure understanding of client needs and meet or exceed expectations.
  10. Organize team meetings as needed.
Education and Experience
  • 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.
  • Familiarity with PV databases (e.g., Argus, ArisG).
Knowledge
  • Understanding of GVP and regulatory standards related to pharmacovigilance.
Skills
  • Prioritization skills.
  • Team management.
  • Organization skills.
  • Team spirit.
  • Methodical approach.
  • Strong communication skills.
  • Decision-making ability.
  • Rigour.
  • Adaptability.
  • Proficiency in Microsoft Office.
  • Fluency in both English and French (oral and written).
Obtenez votre examen gratuit et confidentiel de votre CV.
ou faites glisser et déposez un fichier PDF, DOC, DOCX, ODT ou PAGES jusqu’à 5 Mo.