Preclinical Scientist - Study Monitor

Position summary

Sotio Biotech a.s. is a biopharmaceutical drug development company, focusing on the development of innovative oncology therapies. For our preclinical development pipeline consisting of multiple biologic drug candidates we want you as Preclinical Scientist - Study Monitor.

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 pharmacokinetic and toxicology studies with new drug candidates, mostly 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 (Biology, Physiology, Pharmaceutics, Veterinary Medicine, etc).
PhD in 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.

Location

Position is based in Prague, Czech Republic.

Mám zájem Apply

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Preclinical Scientist - Study Monitor

Position summary

Key Activities and Responsibilities

Competences, Skills and Qualification

Location

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