Lead Global PV Physician – Therapeutic Dermatology

Galderma Services Spain, S.L.

Barcelona

Híbrido

EUR 120.000 - 180.000

Jornada completa

14 días+
Generador de candidaturas

Una candidatura completa en un minuto — currículum adaptado y carta de presentación, listos para enviar.

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Ventajas ofrecidas por este puesto de trabajo

Hybrid working model

Descripción de la vacante

Galderma seeks a Global Pharmacovigilance Risk Minimization Physician to join our Therapeutic Dermatology team in Barcelona. Lead post‑marketing safety activities for Nemluvio and other TD products, ensuring benefit‑risk assessment and regulatory compliance.

Work across Clinical Development, Medical Affairs, Regulatory, Quality, and Commercial teams globally, developing Risk Management Plans and overseeing safety data and PV QMS with inspection readiness.

Formación

  • Medical degree required with extensive pharmacovigilance experience.
  • Expertise in signal detection, safety surveillance, and risk management.
  • Experience supporting regulatory inspections, inspection readiness, CAPA and QMS.
  • Dermatology/pharmacovigilance in biologics is highly desirable.

Responsabilidades

  • Lead post‑marketing safety activities for TD Galderma products, with primary focus on Nemluvio.
  • Oversee benefit‑risk assessments and management of safety risks across global markets.
  • Lead signal detection, validation, evaluation, and escalation using safety data.
  • Develop and maintain Risk Management Plans (RMPs) and risk minimization strategies.
  • Collaborate with Clinical Development, Medical Affairs, Regulatory, Quality, and Commercial teams.

Conocimientos

Medical expertise
Post‑marketing safety
Signal detection
Risk management
Regulatory inspections
QMS
Dermatology experience
Fluent English

Educación

Medical Degree (MD or equivalent)

Descripción del empleo

Galderma seeks a Global Pharmacovigilance Risk Minimization Physician to join our Therapeutic Dermatology team in Barcelona. Lead post‑marketing safety activities for Nemluvio and other TD products, ensuring benefit‑risk assessment and regulatory compliance.

Work across Clinical Development, Medical Affairs, Regulatory, Quality, and Commercial teams globally, developing Risk Management Plans and overseeing safety data and PV QMS with inspection readiness.

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