ENGLISH SPEAKING ACTIVITY ASSISTANT

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

Résumé du poste

A leading company in pharmacovigilance is seeking a dedicated Pharmacovigilance Specialist to oversee compliance and safety data management. The role involves training junior staff, managing client projects, and ensuring regulatory adherence. Ideal candidates will have a pharmacy degree and extensive experience in pharmacovigilance.

Qualifications

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

Responsabilités

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

Connaissances

Team management

Organizational skills

Good communication skills

Decision-making ability

Adaptability

Formation

Pharmacy degree

Outils

Microsoft Office

PV databases (e.g., Argus, ArisG)

Description du poste

The provided job description contains essential information but lacks proper formatting and clarity in some areas. Here is a refined version with improved structure and readability:

Client:

ProductLife Group

Location:

Job Category:

Other

EU work permit required:

Yes

Job Reference:

2673119118827192320327687

Job Views:

2

Posted:

16.05.2025

Job Description:

PLG is seeking a dedicated Pharmacovigilance Specialist - Case Processing to join our hub. The role involves overseeing and collaborating closely with our PV team to ensure compliance with regulatory standards and accurate safety data management.

Responsibilities:

1. Serve as the key trainer for junior team members to enhance quality and expand knowledge in PV case processing.
2. Review and identify areas for improvement.
3. Provide expertise and act as SME for the team, ensuring clear understanding of tasks by case management staff.
4. Manage larger client projects and serve as the single point of contact for clients.
5. Monitor client KPIs.
6. Support in resolving NC/CAPA issues, identify root causes, and implement improvements.
7. Perform Quality Control/Medical Review and support the team to ensure regulatory compliance.
8. Participate in audits and inspections as needed.
9. Understand client needs and ensure expectations are met or exceeded.
10. Organize team meetings as required.

Education and Experience:

• Pharmacy degree.
• 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.
• Familiarity with PV databases (e.g., Argus, ArisG).

Knowledge:

• Understanding of GVP and regulatory standards related to pharmacovigilance.

Skills:

• Sense of priorities.
• Team management.
• Organizational skills.
• Team spirit.
• Methodical approach.
• Good communication skills.
• Decision-making ability.
• Rigour.
• Adaptability.
• Proficiency in Microsoft Office.
• Fluent in both English and French (oral and written).