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