Playworker

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

Résumé du poste

A leading company in pharmacovigilance is looking for a dedicated Pharmacovigilance Specialist to oversee compliance and safety data. The successful candidate will manage projects, train junior staff, and ensure regulatory standards are met. This role requires strong organizational and communication skills, along with significant experience in the field.

Qualifications

• Minimum 5-10 years experience in pharmacovigilance or data management.
• 5+ years experience in the field.

Responsabilités

• Train junior team members on PV case processing.
• Manage larger client projects and monitor KPIs.
• Perform Quality Control and participate in audits.

Connaissances

Team management

Organizational skills

Good communication skills

Decision-making ability

Rigour and adaptability

Sense of priorities

Methodical approach

Team spirit

Formation

Pharmacy graduate

Outils

Microsoft Office

PV databases

Description du poste

PLG is looking for a dedicated Pharmacovigilance Specialist - Case Processing to join our hub. The successful candidate will oversee and work 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 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 the case management team.
4. Manage larger client projects and act as the 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 or exceed expectations.
10. Organize team meetings as requested.

Education and Experience

• Pharmacy graduate.
• Minimum 5-10 years experience working for service providers, preferably in data entry, management, or pharmacovigilance.
• Previous experience of 5+ years in the field.

Technical Skills

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

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