Salima Kassam Mrpharms

Salima Kassam MRPharmS has extensive experience in the pharmaceutical industry, holding key roles focused on quality assurance and regulatory compliance. Currently serving as a Responsible Person at Clovis Oncology since June 2019, Salima also acts as a Back Up for Responsible Person/import at Galapagos since September 2021. Previous positions include GDP Consultant roles at Takeda, TESTERWORLD LIMITED, and Curium Pharma, emphasizing remediation efforts and compliance with quality management systems. Prior experience includes directing quality assurance at CBRE for Novartis and serving as QA Director Distribution at Alexion Pharmaceuticals. Salima holds a Bachelor of Science (BSc) in Pharmaceutical Sciences from London Metropolitan University, obtained from 1996 to 1999.