Pharmacovigilance Activity Manager- Case Processing 381

ProductLife Group; Lille; Sur place; EUR 45 000 - 75 000; Plein temps

Résumé du poste

An innovative firm is seeking a dedicated Pharmacovigilance Activity Manager to lead a team in ensuring compliance with regulatory standards and managing client projects. This role involves training junior members, conducting quality control, and acting as a subject matter expert. With a focus on continuous improvement and client satisfaction, you will have the opportunity to influence the quality of safety data management in a dynamic environment. If you are passionate about pharmacovigilance and possess strong leadership skills, this position offers a rewarding challenge.

Qualifications

• 5-10 years experience in pharmacovigilance or related fields.
• Proficiency in Microsoft Office and PV databases.

Responsabilités

• Train junior team members and enhance the quality of PV case processing.
• Manage client projects and monitor KPIs to ensure compliance.

Connaissances

Team Management

Communication

Methodical Approach

Decision Making

Prioritization

Rigour

Fluency in English

Fluency in French

Formation

Pharmacy Degree

Outils

Microsoft Office

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

Description du poste

PLG is looking for a dedicated Pharmacovigilance Activity Manager- Case Processing to join our hub to oversee and work closely with our PV team to ensure compliance with regulatory standards and accurate safety data.

Responsibilities

• Key trainer for junior team members to increase quality and expand knowledge of PV case processing
• Review and identify areas of improvement
• Provide expertise and act as SME for the team, ensuring understanding of tasks by case management team
• Manage larger client projects and act as single point of contact for the client
• Monitor client KPI
• Support in the resolution of NC / CAPA, identify RCA and implement improvements
• Perform Quality Control / Medical Review and provide support to the team where necessary to ensure regulatory compliance
• Participate in audits and inspections as required
• Ensure understanding of client needs and ensure expectations are met and exceeded
• Organise team meetings as requested

Education and Experience

• Education : 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).
• Previous experience working to deadlines
• Knowledge : Understanding of GVP and regulatory standards related to pharmacovigilance.

Skills

• Sense of priorities
• Team Management
• Team Spirit
• Methodical
• Communicant
• Ability to make decisions
• Rigour
• Microsoft office
• Fluent in both English and French (Oral and Written)