ENGLISH SPEAKING ACTIVITY ASSISTANT

JR France; La Rochelle; À distance; EUR 50 000 - 70 000; Plein temps

Résumé du poste

A leading company is seeking a dedicated Pharmacovigilance Specialist to oversee compliance with regulatory standards and manage safety data. Responsibilities include training team members, managing client projects, and ensuring quality control. The ideal candidate will have extensive experience in pharmacovigilance and proficiency in relevant databases.

Qualifications

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

Responsabilités

• Serve as a key trainer for junior team members.
• 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

Good communication

Decision-making ability

Fluency in English

Fluency in French

Formation

Pharmacy graduate

Outils

Microsoft Office

PV databases

Description du poste

Client:

ProductLife Group

Location:

Virtual job fairs

Job Category:

Other

EU work permit required:

Yes

Job Reference:

2673119118827192320327630

Job Views:

2

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 a 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 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 meet/exceed expectations.
10. Organize team meetings as requested.

Education and Experience:

• Pharmacy graduate.
• 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).
• 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, Good communication, Decision-making ability, Rigour, Adaptability, Proficiency in Microsoft Office, Fluency in English and French (oral and written).

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