Pharmacovigilance Team Lead (French Speaker)

buscojobs España; Toledo; Presencial; EUR 40.000 - 60.000; Jornada completa

Descripción de la vacante

A leading company in the pharmaceutical sector is seeking a Case Specialist Team Lead to oversee the pharmacovigilance team. This role involves managing workload, ensuring compliance with regulatory standards, and fostering team development. The ideal candidate will have a strong pharmaceutical background and experience in drug safety.

Formación

• Experience in coordinating workload and activity management.
• Deep knowledge of pharmacovigilance principles.
• Fluent in both English and French (oral and written).

Responsabilidades

• Plan the workload and assign tasks.
• Ensure compliance with regulatory standards.
• Perform QC and medical evaluations.

Conocimientos

Organization skills

Good communication skills

Team spirit

Rigour

Methodical approach

Ability to make decisions

Sense of priorities

Educación

Pharmaceutical background

Minimum 3 years of PV case processing experience

Herramientas

Microsoft Office

Safety databases (Safety Easy – Argus)

Descripción del empleo

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Client : ProductLife Group

Location :

Job Category : Other

EU work permit required :

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Job Reference :

209998124528173056032460

Job Views :

Posted : 31.03.2025

Expiry Date : 15.05.2025

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Job Description :

PLG is looking for a dedicated Case Specialist Team Lead / LPPV to join our hub to oversee and work closely with our PV team to ensure compliance with regulatory standards and accurate safety data.

Responsibilities :

• Plan the workload.
• Assign tasks in a timely manner.
• Organize planning and monitoring of specific projects.
• Check that all files are properly handled and reorganize workload as necessary.
• Ensure line management of the Case Specialist team.
• Follow up with training and development plans for the team.
• Perform QC and medical evaluations.
• Be accountable for entrusted activities.
• Participate in process implementation related to the project.
• Handle local responsibilities (LPPV).

Education and Experience :

• Experience in coordinating workload and activity management.
• Minimum 3 years of PV case processing experience is a plus.
• Experience communicating directly with clients.
• Prior experience in a similar position is preferred.
• Pharmaceutical background with strong understanding of GVP, GCP, FDA, and regulatory requirements related to drug safety.
• Deep knowledge of pharmacovigilance principles, adverse event reporting, causality assessment.
• Knowledge of safety databases (Safety Easy – Argus).

Skills :

• Sense of priorities.
• Organization skills.
• Team spirit.
• Methodical approach.
• Good communication skills.
• Ability to make decisions.
• Rigour.
• Proficiency in Microsoft Office.
• Fluent in both English and French (oral and written).