Labcorp Drug Development
Maidenhead SL6, UK
Senior Medical Writer – Regulatory Writing – EMEA, Remote Are you an experienced Medical Writer with extensive experience writing clinical study reports and protocols? Perhaps you are looking to broaden your regulatory writing experience across late phase studies? Want to join a global team, where you can develop your career and be involved in collaborative discussions on the drug development process, with other experienced Medical Writers? The Senior Medical Writer will be responsible for the preparation and coordination of clinical study protocols and clinical study reports (CSRs), and other documents as needed, across global projects. As a leading contract research organization (CRO), Labcorp Drug Development provides comprehensive drug development solutions for a range of industries. Our services cover the preclinical, clinical and post-market phases of drug development, the product life cycles for medical device and diagnostics and...