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Safety Physician Oncology

Debiopharm · Lausanne

New
CDI 🇬🇧 English
Microsoft 365

Job description

About the role

We are seeking a Safety Physician Oncology to join our Clinical Safety and Pharmacovigilance team in Lausanne. In this position you will actively manage and evaluate safety risks of oncology and antibiotic products in development, and support early‑phase studies in healthy volunteers together with the Clinical Pharmacology & Drug Metabolism team.

Key responsibilities

  • Evaluate and establish the safety profile of products in collaboration with internal experts and external partners.
  • Provide medical input for accelerated‑approval documents, investigator brochures and development safety update reports.
  • Conduct safety surveillance, including medical review of individual cases and ongoing signal detection.
  • Oversee outsourced pharmacovigilance activities and ensure quality of vendor deliverables.
  • Lead the design and implementation of a signal‑detection tool together with clinical medicine, biometry and pharmacology functions.

Required profile

  • Medical Doctor with experience in clinical safety during early drug development in a global pharma or CRO environment.
  • Minimum five years of direct clinical safety experience in the biotech/pharmaceutical industry.
  • Experience in oncology drug development is an asset.
  • Strong leadership, collaboration and decision‑making abilities.
  • Proficiency with Microsoft 365 and a strong appetite for digital tools.

What we offer

  • International, highly dynamic environment with a long‑term vision.
  • Cross‑functional collaboration at the forefront of oncology and anti‑bacterial science.
  • Exposure to a wide variety of areas and functions within clinical development.
  • Culture that values innovation, entrepreneurship and equal‑pay certification.

Questions fréquentes

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Le contrat proposé est un CDI basé à Lausanne.
Source : ats:workable

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Published 3 hours ago

Expires 1 month from now

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Debiopharm

Lausanne