ENGLISH SPEAKING ACTIVITY ASSISTANT

JR France; Paris; Sur place; EUR 50 000 - 70 000; Plein temps

Résumé du poste

A leading company in pharmacovigilance is seeking a dedicated Pharmacovigilance Specialist in Paris. The role involves overseeing compliance with regulatory standards, managing client projects, and training junior team members. Candidates should have extensive experience in pharmacovigilance and proficiency in Microsoft Office. Fluency in English and French is essential.

Qualifications

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

Responsabilités

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

Connaissances

Team Management

Organization skills

Decision-making ability

Adaptability

Fluent in English

Fluent in French

Formation

Pharmacy graduate

Outils

Microsoft Office

PV databases

Description du poste

ENGLISH SPEAKING ACTIVITY ASSISTANT, Paris

Client:

ProductLife Group

Location:

Paris, France

Job Category:

Other

EU work permit required:

Yes

Job Reference:

267311911882719232032760

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. Serve as the key trainer for junior team members to improve 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 the 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 meet or exceed expectations.
10. Organize 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).
• 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 approach, Communicative, Decision-making ability, Rigor, Adaptability, Microsoft Office proficiency, Fluent in both English and French (oral and written).

Additional Notes:

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