Regulatory Affairs - Jobs

Responsible for assisting in the development and maintenance of a clinical quality management framework including development of processes and standards, training, and execution of compliance activities....  More Details

external party personnel (e.g. CROs) to analyze, define and document data and information flows impacting clinical operations and data management   Skills    Soft Skills - Strong analytical skills applied to understanding business functionality and translating them into application requirements - Ability to create compelling business cases with accurate...  More Details

least 8 years of relevant project management experience; or equivalent. Familiarity with all aspects of drug development, including clinical development, regulatory affairs, pharmaceutical development, and manufacturing Solid knowledge of the drug development and...  More Details

Vertex Pharmaceuticals is looking for a Quality Lead- GMP Auditing to join our Quality Compliance Management team. The Quality Lead (GMP Auditor) of Quality Compliance Management is responsible for the compliance oversight and monitoring of GMP service provider activities. Responsibilities - Demonst...  More Details