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ENGLISH SPEAKING ACTIVITY ASSISTANT

JR France

Toulon

Sur place

EUR 50 000 - 70 000

Plein temps

Il y a 4 jours
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Résumé du poste

A leading company in pharmacovigilance is seeking a dedicated Pharmacovigilance Specialist to oversee compliance and safety data. The role involves training junior staff, managing client projects, and ensuring regulatory adherence. Candidates should have extensive experience in the field and proficiency in relevant software.

Qualifications

  • Minimum 5-10 years working for service providers.
  • Previous experience in pharmacovigilance preferred (5+ years).

Responsabilités

  • Key trainer for junior team members to increase quality.
  • Manage larger client projects and act as a single point of contact.
  • Perform Quality Control/Medical Review and support regulatory compliance.

Connaissances

Team Management
Organization skills
Communicant
Adaptability
Sense of priorities
Rigour

Formation

Pharmacy graduate

Outils

Microsoft Office
PV databases

Description du poste

Client:

ProductLife Group

Location:

Toulon, France

Job Category:

Other

Online job hunting tools

-

EU work permit required:

Yes

Job Reference:

2673119118827192320327650

Job Views:

1

Posted:

16.05.2025

Job Description:

PLG is looking for a dedicated Pharmacovigilance Specialist - Case Processing to join our hub. The role involves overseeing and working closely with our PV team to ensure compliance with regulatory standards and accurate safety data.

Responsibilities:
  1. Key trainer for junior team members to increase quality and expand knowledge of PV case processing.
  2. Review and identify areas of improvement.
  3. Provide expertise and act as SME for the team, ensuring understanding of tasks by the case management team.
  4. Manage larger client projects and act as a single point of contact for the client.
  5. Monitor client KPIs.
  6. Support in the resolution of 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 that expectations are met or exceeded.
  10. Organize team meetings as requested.
Education and Experience:

Education: Pharmacy graduate

Experience: Minimum 5-10 years 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)
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