German Medical Information Consultant – Pharma Expert

QbD Group | Spain

Madrid

Presencial

EUR 55.000 - 75.000

Jornada completa

14 días+
Generador de candidaturas

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Descripción de la vacante

QbD Group | Spain seeks an experienced Medical Information professional to manage inquiries, literature searches, and regulatory liaison. You will contribute to pharmacovigilance and regulatory activities, ensuring high-quality medical information delivery across therapeutic areas.

The role requires strong German/English language skills, expertise in medical literature, and collaboration with PV, RA, Clinical teams. Opportunities to shape MI processes and adopt AI tools are available.

Formación

  • Bachelor's degree in Life Sciences or related field.
  • Master's degree in Pharmaceutical Industry or related; desirable.
  • PhD in life sciences is a plus.
  • Experience in Pharmaceutical Industry (Medical Affairs, Regulatory, Medical Information and/or Pharmacovigilance).
  • Strong scientific/medical literature management experience.
  • Clinical trials knowledge and ability to interpret literature.

Responsabilidades

  • Handle MI inquiries and literature provision.
  • Collaborate with PV, RA, Clinical and other departments.
  • Review promotional materials from a scientific/medical perspective.
  • Conduct EMA and authority searches and safety literature monitoring.
  • Evaluate AI-based tools to optimise MI workflow.
  • Support onboarding and training for MI trainees.

Conocimientos

Scientific literature management
German and English proficiency
Knowledge of scientific databases
Clinical trials knowledge
Analytical mindset

Educación

Bachelor's degree in Life Sciences or related
Master's degree in Pharmaceutical Industry or related (Desirable)
PhD in life sciences (Plus)

Herramientas

PubMed
Medline
ClinicalTrials.gov

Descripción del empleo

QbD Group | Spain seeks an experienced Medical Information professional to manage inquiries, literature searches, and regulatory liaison. You will contribute to pharmacovigilance and regulatory activities, ensuring high-quality medical information delivery across therapeutic areas.

The role requires strong German/English language skills, expertise in medical literature, and collaboration with PV, RA, Clinical teams. Opportunities to shape MI processes and adopt AI tools are available.

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