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Oznamy

Sotio a.s. - Prague, Czech - ŠP VVL, HP

07.02.2019   Kariéra
Position: Preclinical Scientist / Study Monitor
Department: Preclinical Development
Responsible To: Director of Preclinical Safety
Location: Prague, Czech Republic
Employment Type: Full time employment

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 Preclinical Scientist / Study Monitor.
Position is based in Prague, Czech Republic.

Key Activities and Responsibilities:

  • Participation in project work as a scientist in preclinical safety within preclinical development department of Sotio and international collaboration teams.
  • Participation in design, planning and monitoring of preclinical pharmacokinetic and safety studies with new drug candidates, conducted at contracted laboratories.
  • Scientific evaluation of results, work with scientific literature.
  • Presenting, interpreting and discussing the study results.
  • Continual development of expertise in areas of preclinical safety and drug development.

Competences, Skills and Qualification:

  • Degree in veterinary medicine or similar (biology, pharmaceutics).
  • PhD in relevant area is welcomed but not a must.
  • 3 to 5 years of experience in pharmaceutical or academic research, efficacy or safety studies.
  • Knowledge of biology and physiology.
  • Highly efficient in work with scientific literature and scientific writing, preparation of presentations, tables, graphs, Microsoft Office.
  • Also welcomed are overall understanding of the drug development process and work under SOP and GLP (or GCP).
  • Excellent communication skills in international research environment are essential.
  • Fluent spoken and written English are essential.

Contact:
hr@sotio.com
praslicka@sotio.com

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