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