Trainee - Toxicology Study Director
Apply locations: Verona
Job type: Full time | Posted on: Yesterday | Requisition ID: JOB ID-12339
Evotec offers an exciting opportunity in the Safety Assessment Department in Verona for an internship as a 'Toxicology Study Director' with the following characteristics:
Requirements
* Master's degree in Biology, Biotechnology, Chemistry, Pharmaceutical Technologies, or Pharmacy;
* Interest in activities involving primary cell cultures, cell lines, bacterial cultures, and genetic toxicology testing (preferential).
* Interest in general toxicology studies across different test systems;
* Basic knowledge of MS Office, 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 management of Toxicology studies as a Study Director;
* Fellowship and free lunch;
* Learning the process of preclinical development of new molecules, including study protocol preparation, supervision of experimental steps, and data review and evaluation;
* Professional training through reading and discussing regulatory guidelines: ICH, OECD, EMA, FDA;
* Practical, on-the-job training aimed at achieving complete autonomy in laboratory activities, data interpretation, reporting, and submission.
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Opportunità in italiano
Evotec offre un’interessante opportunità nel Dipartimento di Safety Assessment di Verona per un tirocinio in "Toxicology Study Director" con le seguenti caratteristiche:
Requisiti
* Laurea Magistrale in Biologia, Biotecnologia, CTF, Farmacia;
* Interesse per attività con colture cellulari primarie, linee cellulari, colture batteriche e test di tossicologia genetica (preferenziale);
* Interesse in studi di tossicologia generale con differenti test systems;
* Conoscenza di base del pacchetto MS Office, preferibilmente avanzata in Excel.
Il progetto formativo prevede:
* Affiancamento completo a tutor scientifici per 6 mesi;
* Borsa di studio e mensa gratuita;
* Apprendimento del processo di sviluppo preclinico di nuove molecole, inclusa la preparazione di protocolli, supervisione delle fasi sperimentali, revisione e valutazione dei dati;
* Formazione su linee guida regolatorie: ICH, OECD, EMA, FDA;
* Training pratico on the job con autonomia completa nelle attività di laboratorio, interpretazione, reportistica e presentazione dei dati.
FR: In accordo con la politica di Diversità, Evotec valuta tutte le candidature con uguali opportunità, incluse quelle di persone con disabilità.
ENG: As part of our Diversity policy, Evotec considers all applications equally, including those from people with disabilities.
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