Info
03 May 2022
Employee, 100%
Required minimum profile
- PhD in toxicology, pharmacology, immunology, veterinary medicine, or related disciplines
- At least 3-5 years of relevant industry experience in early and late-stage drug development projects, preferentially as the Preclinical Safety Project Team representative
- Knowledgeable about GLP policies and/or regulatory nonclinical testing requirements for pharmaceutical development of biotherapeutics and small molecules
- Experienced in the preparation of regulatory documents for submission to health authorities
- C1 level in English (verbal and written communication) mandatory
Contact
STALICLA SA
Lynn Durham
Avenue de Sécheron 15
1202 Genève
Phone: +41 22 545 12 42
No recruitment agencies please
Industry
Science and researchYear of foundation
2017