Pharmacovigilance Team Lead (French Speaker)

buscojobs España; Cádiz; 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 a pharmacovigilance team. The role involves ensuring compliance with regulatory standards, managing workload, and facilitating team development. Ideal candidates will have a strong pharmaceutical background and experience in case processing.

Formación

• Min 3 years PV case processing experience is a plus.
• Experience of communicating directly with clients.
• Prior experience in a similar position is preferred.

Responsabilidades

• Plans the workload and assigns tasks.
• Ensures compliance with regulatory standards.
• Performs QC and medical evaluation.

Conocimientos

Sense of priorities

Organization

Team Spirit

Methodical

Communicant

Ability to make decisions

Rigour

Fluent in both English and French

Educación

Pharmaceutical background

Herramientas

Microsoft Office

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 :

1. Plans the workload.
2. Assigns the tasks on a timely manner
3. Organize the planning and monitoring of one specific project
4. Check that all files are properly handled as the day progresses and ensure that the workload is reorganized as necessary
5. Ensure the line management of Case Specialist team
6. Follow up with trainings and development plan of team
7. Perform QC and medical evaluation
8. To be accountable for the activities entrusted for the position.
9. Participate in the implementation of processes related to the project
10. Local responsibilities (LPPV)

Education and Experience

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

Skills

1. Sense of priorities
2. Organization
3. Team Spirit
4. Methodical
5. Communicant
6. Ability to make decisions
7. Rigour
8. Microsoft office
9. Fluent in both English and French (Oral and Written)