Les offres d'emploi : Professions sociales - Santé ...

Key Responsibilities:

- Participate in the handling of Serious Adverse Event (SAE) reports.
- Provide an excellent support to Development and Marketed product studies.
- Liaison with the Manager, Trials Safety Surveillance and the Clinical Safety Group in Global Drug Safety.
- Participate in the drafting of various safety reports or documents to comply with Federal, European and International Regulatory requirements and/or internal needs.
- Ensure the relevance and the quality of the information on the Clinical Safety data used for decisions on risk/minimization and assessment.

Your Profile:

- Possess a Degree in Life Sciences with good medical knowledge or fully qualified Nurse or Pharmacist.
- Minimum 3 year-experience in pharmaceutical industry, of which 1-2 years spent in Drug Safety.
- Previous experience in Clinical Operations or Trial Safety would be an advantage.
- Good communication skills, including good written and spoken English.
- Knowledge of databases used by Clinical Operations, including good understanding of Safety data capture in clinical trial settings.
- Working knowledge of European Regulations governing Suspected Adverse Reaction report collection, evaluation, processing, and submission for both investigational medicinal products and marketed product would be helpful.
- Possess valid Swiss working permission or EU Citizenship required.



MICHAEL PAGE...