Activity Leader

JR France; Neuilly-sur-Seine; Sur place; EUR 50 000 - 70 000; Plein temps

Résumé du poste

A leading company is seeking a dedicated Pharmacovigilance Specialist to oversee compliance and safety data. This role involves training junior members, managing client projects, and ensuring regulatory standards are met. Candidates should have significant experience in pharmacovigilance and strong communication skills in both English and French.

Qualifications

• Minimum 5-10 years of experience with service providers.
• Previous experience in pharmacovigilance preferred.

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

Communication

Decision-Making

Adaptability

Formation

Pharmacy graduate

Outils

Microsoft Office

PV databases

Description du poste

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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.

Responsibilities

1. Serve as the key trainer for junior team members to enhance quality and knowledge in 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 clients.
5. Monitor client KPIs.
6. Support in resolving NC/CAPA issues, 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 needed.

Education and Experience

• Pharmacy graduate.
• Minimum 5-10 years of experience working with 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, organization skills, team spirit, methodical approach, communication skills, decision-making ability, rigor, adaptability.
• Fluent in both English and French (oral and written).