Claudia Selck

Senior preclinical scientist with hands-on experience in regulatory documentation and scientific writing, now seeking to transition into a role in Regulatory Affairs or start a new exciting position as a Senior Scientist.Proven track record in designing and implementing efficacy/safety in vitro assays in accordance with GxP principles and in close collaboration with Regulatory Affairs, QA/QC, CMC and external CROs. Preparation of key sections of regulatory documents and actively building regulatory expertise by formal training.Recognized for strong technical writing, effective coordination of cross-functional projects and excellent communication skills.