Trainee (Pharmacokinetic studies of biosimilars in trial registries: retrieval and evaluation)

The European Medicines Agency (EMA) is seeking a trainee to conduct research on biosimilar medicines through public clinical trial registries and internal EMA regulatory resources, leading to a publication. The successful candidate will gain in-depth knowledge of EMA's Clinical Trials Information System and public clinical trial registries, as well as biosimilar and overall medicine development and regulatory assessment and authorisation.

Requirements

• Enjoy full rights as a citizen of a European Union Member State or Iceland, Lichtenstein, and Norway
• Possess a university degree in clinical pharmacology, biomedical sciences, or any other life sciences
• Thorough knowledge of English (at least level C1) and good knowledge of other official EU language (at least B2)
• Strong analytical skills, diligent and systematic approach to work, high attention to detail, and solid understanding of scientific methodology

Benefits

• Monthly stipend of €2,049.77 for a full-time traineeship
• Travel contribution upon joining the Agency
• Mentorship from an experienced colleague at the Agency