Preclinical Safety Scientist - Study Monitor

Position Summary

Sotio a.s. is a biopharmaceutical development company, focusing on the development of innovative oncology therapies. For our early development pipeline, consisting of small molecule and biologic drug candidates, we want you as a Preclinical Safety Scientist / Study Monitor.

 

The position is based in Prague, Czech Republic.

Key Activities and Responsibilities

  • Participation in project work as a scientist in preclinical safety and toxicology within Preclinical Development department and international collaboration teams.
  • Design, preparation, and monitoring of preclinical pharmacokinetics and toxicology studies with new drug candidates, conducted at contracted laboratories.
  • Active in generation and review of study plans, monitor study events, review of study reports.
  • Presenting, discussing, and co-interpreting study results.
  • Continuous development of expertise in areas of preclinical safety and drug development.
  • Reporting to Director of Preclinical Safety.

Competences, Skills and Qualification

  • Degree in biological sciences (Veterinary Medicine, Biology, Physiology, Pharmaceutics, etc).
  • PhD in the relevant area welcomed.
  • Knowledge of animal and/or human biology and physiology is essential.
  • At least 3 years of experience in pharmaceutical or academic research.
  • Highly efficient in work with scientific literature and scientific writing, preparation of presentations, tables, graphs, Microsoft Office.
  • Fluent spoken and written English and excellent communication skills in international research environment are essential.

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