ENGLISH SPEAKING ACTIVITY ASSISTANT

JR France; Chalon-sur-Saône; Sur place; EUR 50 000 - 70 000; Plein temps

Résumé du poste

A leading company in pharmacovigilance seeks a dedicated Pharmacovigilance Specialist - Case Processing. You will oversee compliance with regulatory standards and ensure accurate safety data while managing client projects and training junior team members. This role requires a Pharmacy graduate with extensive experience in pharmacovigilance and strong organizational skills. Fluency in English and French is essential.

Qualifications

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

Responsabilités

• Serve as key trainer for junior team members.
• Manage larger client projects and act as single point of contact.
• Perform Quality Control/Medical Review.

Connaissances

Team Management

Organization skills

Team Spirit

Methodical approach

Communicative

Decision-making ability

Rigour

Adaptability

Proficiency in Microsoft Office

Fluent in English

Fluent in French

Formation

Pharmacy graduate

Outils

Microsoft Office

PV databases

Description du poste

Social network you want to login/join with:

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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:

2673119118827192320327682

Job Views:

2

Posted:

16.05.2025

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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. Serve as the key trainer for junior team members to enhance quality and expand knowledge of PV case processing.
2. Review cases and identify areas for improvement.
3. Provide expertise and act as SME for the team, ensuring understanding of tasks by case management team.
4. Manage larger client projects and act as the 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:

• Pharmacy graduate with minimum 5-10 years of 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 approach, Communicative, Decision-making ability, Rigour, Adaptability, Proficiency in Microsoft Office, Fluent in both English and French (Oral and Written).