TRABAJO REGULATORY AFFAIRS STUDY START BARCELONA, BARCELONA

Response documents, study protocols, psrs, etc... • identify regulatory risks and propose mitigations to lead rpm and cross-functional teams...

Organizes regulatory information, logs and tracking... maintains regulatory files/database and chronologies in good order... participate in the product development...

The lab forms part of international consortia focused on advancing research in regulatory genomics, single cell genomics, and human genetics...

Provide expert input on study protocols and methodological strategy... stay current on regulatory and methodological developments and promote best practices...

Educating clinical staff on regulatory requirements, quality standards and good practices... support regulatory inspections (fda, ema), including preparation, hosting...

P rovide expert scientific input into the preparation of regulatory documents and interactions with regulatory authorities...     desirable   experience with regulatory...

Experience of global regulatory submissions and interacting with major regulatory agencies... clinical development, medical affairs, regulatory affairs)...

Provide expert scientific input into the preparation of regulatory documents and interactions with regulatory authorities... desirable experience with regulatory...

Your new role do you have experience with biocide product registration and a solid understanding of bpr and reach regulations? at ramboll, we are looking for a dossier...