Pharmacovigilance Team Lead (French Speaker)

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

Descripción de la vacante

A leading pharmaceutical company is seeking a dedicated Case Specialist Team Lead to oversee the pharmacovigilance team. This role involves ensuring compliance with regulatory standards, managing workload, and training team members. Candidates should have a strong pharmaceutical background and experience in case processing.

Formación

• Experience in coordinating workload and activity management.
• Prior experience in a similar position is preferred.
• Deep knowledge of pharmacovigilance principles and regulatory requirements.

Responsabilidades

• Plan the workload and assign tasks in a timely manner.
• Ensure compliance with regulatory standards and accurate safety data.
• Participate in the implementation of project-related processes.

Conocimientos

Organization skills

Strong communication skills

Decision-making ability

Team spirit

Rigour

Methodical approach

Sense of priorities

Educación

Pharmaceutical background

Minimum 3 years of PV case processing experience

Herramientas

Safety databases (Safety Easy – Argus)

Microsoft Office

Descripción del empleo

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Client : ProductLife Group

Location : Job Category :

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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 :

1. Plan the workload.
2. Assign tasks in a timely manner.
3. Organize the planning and monitoring of specific projects.
4. Check that all files are properly handled and reorganize workload as necessary.
5. Ensure line management of the Case Specialist team.
6. Follow up with training and development plans for the team.
7. Perform QC and medical evaluations.
8. Be accountable for the activities entrusted for the position.
9. Participate in the implementation of project-related processes.
10. 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 a strong understanding of GVP, GCP, FDA, and regulatory requirements related to drug safety.
• Deep knowledge of pharmacovigilance principles, adverse event reporting, and causality assessment.
• Knowledge of safety databases (Safety Easy – Argus).

Skills :

• Sense of priorities.
• Organization skills.
• Team spirit.
• Methodical approach.
• Strong communication skills.
• Decision-making ability.
• Rigour.
• Proficiency in Microsoft Office.
• Fluent in both English and French (oral and written).

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