Social network you want to login/join with:
col-narrow-left
Client:
ProductLife Group
Location:
Job Category:
Other
-
EU work permit required:
Yes
col-narrow-right
Job Reference:
2673119118827192320327625
Job Views:
1
Posted:
16.05.2025
col-wide
Job Description:
PLG is seeking a dedicated Pharmacovigilance Specialist - Case Processing to join our hub. The role involves overseeing and collaborating 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 processes and identify areas for improvement.
- Provide expertise and act as SME for the team, ensuring understanding of tasks by case management staff.
- Manage larger client projects and act as the primary contact for clients.
- Monitor client KPIs.
- Support in resolving NC/CAPA, identify RCA, and implement improvements.
- Perform Quality Control/Medical Review and support the team to ensure regulatory compliance.
- Participate in audits and inspections as required.
- Understand client needs and ensure their expectations are met or exceeded.
- Organize team meetings as needed.
Education and Experience:
- 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).
Knowledge:
- Understanding of GVP and regulatory standards related to pharmacovigilance.
Skills:
- Prioritization, team management, organization skills, team spirit, methodical approach, communication skills, decision-making ability, rigor, adaptability, proficiency in Microsoft Office, fluency in English and French (oral and written).