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Activity leader, H/F

JR France

Le Plessis-Robinson

Sur place

EUR 50 000 - 70 000

Plein temps

Il y a 5 jours
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Résumé du poste

A leading company is seeking a dedicated Pharmacovigilance Specialist to oversee compliance and safety data management. The role involves training team members, managing client projects, and ensuring regulatory adherence. Ideal candidates will have significant experience in pharmacovigilance and strong technical skills.

Qualifications

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

Responsabilités

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

Connaissances

Team Management
Organization skills
Team Spirit
Methodical
Communicant
Ability to make decisions
Rigour
Adaptability
Microsoft Office

Formation

Pharmacy graduate

Outils

PV databases
Microsoft Office

Description du poste

Social network you want to login/join with:

Activity leader, H/F, le plessis-robinson

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Client:

ProductLife Group

Location:
Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

4452555543080337408327675

Job Views:

1

Posted:

15.05.2025

Expiry Date:

29.06.2025

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Job Description:

PLG is looking for a dedicated Pharmacovigilance Specialist- Case Processing 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 KPIs
  • 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:

  • 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)
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