SOTIO a.s.
SOTIO a.s. is an international pharma/biotech company in Prague, owned by PPF Group, developing new therapies focusing on the treatment of cancer and autoimmune diseases. We pursue this goal through the SOTIO® in-house research, preclinical and clinical development, collaborations with external partners, in-licensing deals, investments and acquisitions. We are now looking for new colleagues into the research department.
The advertised role is in preclinical safety department.
However, there are other research positions available in pharmacology and pharmacokinetics, please see: https://sotio.com/career
Any clarifying questions can be directed to praslicka@sotio.com
The positions are ideal for new PhDs, postdocs and at some cases even for fresh DVMs, biologists, etc.
Please, apply directly from the job advertisement on our website.
The positions are based in Prague, CZ.
Preclinical Safety Scientist - Study Monitor
Position Summary
- For our preclinical development pipeline, consisting of drug candidates for oncology indications, we offer the position of Preclinical Safety Scientist / Study Monitor.
Key Activities and Responsibilities
- Participation in project work as a scientist in preclinical safety and toxicology within the Preclinical Development department and international collaboration teams.
- Design, preparation, and monitoring of preclinical pharmacokinetic 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).
- Ph.D. 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.