Evotec offers an exciting opportunity in the Safety Assessment Department in Verona for an internship in 'Toxicology Study Director' with the following characteristics:

Requirements:
- Master's degree in Biology, Biotechnology, Chemistry and Pharmaceutical Technologies, Pharmacy;
- Interest in activities with primary cell cultures and cell lines, bacterial cultures, genetic toxicology testing will be evaluated as preferential attitude.

- Interest in general toxicology studies in different test systems
- Basic knowledge of MS Office package, preferably advanced in Excel.

The training project includes:

- Full mentorship with scientific mentors for the entire 6-month period.
- cross-training in in-vitro methodologies and managing of Toxicology studies as a Study Director.

- Fellowship and Free Lunch.
- Learning the process of preclinical development of new molecules through preparation of study protocols, supervision of experimental steps, review and evaluation of data.
- Professional training through reading and discussion of regulatory guidelines: ICH, OECD, EMA, FDA

- Practical training, i.e., on-the-job training, with the goal of complete autonomy from the mentor to perform laboratory activities, interpretation, reporting, and data submission for any assays.

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Evotec offre un’interessante opportunità nel Dipartimento di Safety Assessment di Verona per un stage in "Toxicology Study Director', ad un tirocinante con le seguenti caratteristiche:

Requisiti:

• Laurea Magistrale in Biologia, Biotecnologia, CTF, Farmacia;
• Interesse per attività con le colture cellulari primarie e linee cellulari, colture batteriche, test di tossicologia genetica sara’ valutato come interesse preferenziale;
• Interesse in Studi di Tossicologia generale con differenti test systems
• Conoscenza base del pacchetto MS Office, preferibilmente avanzata in Excel.

Il progetto formativo prevede:

• Completo affiancamento a tutor scientifici per l’intero periodo di 6 mesi
• Borsa di studio e mensa gratuito.
• Apprendimento del processo di sviluppo preclinico di nuove molecole attraverso la preparazione di protocolli di studio, supervisione delle fasi sperimentali, revisione e valutazione dei dati.
• Formazione professionale attraverso lettura e discussione di linee guida regolatorie: ICH, OECD, EMA, FDA
• Formazione pratica, ovvero training on the job, con l’obiettivo della completa autonomia dal tutor per l’espletamento delle attività di laboratorio, di interpretazione, reportistica e presentazione dei dati

FR : Dans le cadre de sa politique Diversité, Evotec étudie, à compétences égales, toutes les candidatures dont celles des personnes en situation de handicap.

ENG : In the frame of our Diversity policy, Evotec considers, with equal competences, all applications including people with disabilities.