Your position
You will be involved in all facets of drug safety management, including the processing of adverse event cases, writing case narratives and establishing causality assessments. You will participate in the preparation of pharmacovigilance reports, thus contributing to high quality standards within the organization. You will have responsibilities for your projects and liaise closely with clients and physicians. Some travel activity is required.

Your profile
You hold a university degree in medicine and you have at least 2 years of clinical experience. Excellent command of IT tools is a prerequisite. You are flexible, reliable, detail-oriented and very organized, with excellent written and spoken communication skills in English. You have strong inter-personal skills and appreciate working in a team. You have a convincing personality and the ability to manage multiple tasks. Experience in pharmacovigilance is an additional asset.

Whom to contact
If your experience and interests match the above profile, and you would like to apply for this position, please send your full application documentation to the following:

Dr Véronique Basch
veronique.basch@unitedbiosource.com

United Biosource Corporation
8, avenue des Grandes-Communes
1213 Petit-Lancy/Geneva
Switzerland
Tel + 41 22 596 44 20
Fax+ 41 22 596 44 46
www.unitedbiosource.com
www.hpmgeneva.com