Director Immunogenicity Sciences - Barcelona - Alexion Pharmaceuticals

We are seeking a Director of Immunogenicity Sciences to join our team in Barcelona, Spain. · Developing strategies to address scientific and regulatory priorities that should be integrated to understand and manage immunogenicity-related risks for the successful development of bio ...

Expert Medical Regulatory Writer writes and/or edits under guidance high-quality clinical and safety documents for submission to regulatory authorities to support marketing authorization applications renewals and maintenance activities including complex Clinical Study Reports CSR ...

This position involves writing and/or editing high-quality clinical and safety documents for submission to regulatory authorities. The ideal candidate will have experience in regulatory writing for the pharmaceuticals/healthcare industry and excellent communication skills. · ...

+Job summary · KYMOS GROUP is a medium-size and fast-growing Contract Research Organization (CRO) with headquarters in Spain and laboratories in Spain (Cerdanyola del Vallés- Barcelona), Italy (Monsano-Ancona), and Germany (Frankfurt). It offers comprehensive bioanalytical and CM ...

We are seeking a Principal Medical Regulatory Writer to join our team at Sanofi Global Hub in Barcelona. · ...

Sanofi Global Hub is an internal Sanofi resource organization based in India. · Main responsibilities: · ...

We're partnering with a leading international bioanalytical and drug development organization to recruit a Pharmacokinetic Scientist to join their growing PK/DMPK team. · This is a hands-on scientific role with strong project ownership and client-facing exposure, working across p ...

We are seeking an Expert Medical Regulatory Writer to join our team in Barcelona. · The successful candidate will be responsible for writing and editing high-quality clinical and safety documents for submission to regulatory authorities. · ...

This is an Expert Medical Regulatory Writer position at Sanofi in Barcelona. · ...

Location: Barcelona. · A permanent and full-time position at Sanofi Global Hub in India. · ...

The Principal Medical Regulatory Writer will independently write and/or edit/analyse/compile/summarize high-quality clinical and safety documents for timely submission to regulatory authorities to support marketing authorization applications, · renewals, · and maintenance activit ...