ENGLISH SPEAKING ACTIVITY ASSISTANT

JR France; Cherbourg-en-Cotentin; Sur place; EUR 50 000 - 70 000; Plein temps

Résumé du poste

A leading company is seeking an English Speaking Activity Assistant in Cherbourg-Octeville. This role involves overseeing pharmacovigilance activities, training junior staff, managing client projects, and ensuring compliance with regulatory standards. The ideal candidate will have significant experience in pharmacovigilance and strong organizational skills. Fluency in English and French is required.

Qualifications

• Minimum 5-10 years experience working for service providers.
• Previous experience in data entry, management, or 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 to ensure compliance.

Connaissances

Team Management

Organization skills

Communication

Adaptability

Formation

Pharmacy graduate

Outils

Microsoft Office

PV databases

Description du poste

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ENGLISH SPEAKING ACTIVITY ASSISTANT, Cherbourg-Octeville

Client: ProductLife Group

Location:

Job Category: Other

Virtual job fairs

-

EU work permit required:

Yes

Job Reference:

2673119118827192320327654

Job Views:

1

Posted:

16.05.2025

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)

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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