ENGLISH SPEAKING ACTIVITY ASSISTANT

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

Résumé du poste

A leading company in the pharmaceutical sector is seeking a Pharmacovigilance Specialist - Case Processing. This role involves overseeing a team to ensure compliance with regulatory standards and effective safety data management. The ideal candidate will have extensive experience in pharmacovigilance, strong communication skills, and the ability to manage client relationships effectively. Join us to enhance quality and exceed client expectations.

Qualifications

• Minimum 5-10 years experience in pharmacovigilance.
• Experience in data entry and management.

Responsabilités

• Serve as the key trainer for junior team members.
• Manage larger client projects and act as the main contact.
• Perform Quality Control/Medical Review for compliance.

Connaissances

Prioritization

Organizational skills

Team management

Strong communication

Decision-making

Rigour

Adaptability

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:

2673119118827192320327614

Job Views:

1

Posted:

16.05.2025

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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:

• Serve as the key trainer for junior team members to enhance quality and expand knowledge in PV case processing.
• Review cases and identify areas for improvement.
• Act as SME for the team, ensuring clear understanding of tasks by case management staff.
• Manage larger client projects and act as the main contact for clients.
• Monitor client KPIs.
• Support resolution of NC/CAPA, identify RCA, and implement improvements.
• Perform Quality Control/Medical Review to ensure regulatory compliance.
• Participate in audits and inspections as required.
• Understand and meet client needs, exceeding expectations.
• Organize team meetings as needed.

Education and Experience:

• Pharmacy graduate.
• Minimum 5-10 years experience working for service providers, preferably in pharmacovigilance.
• 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:

• Prioritization and organizational skills.
• Team management and team spirit.
• Methodical approach.
• Strong communication skills.
• Decision-making ability.
• Rigour and adaptability.
• Fluency in English and French (oral and written).