Trabajos regulatory en Southampton - Page 2Crear alertas

Acts as a Global Medical Writing Lead, generally in mid- to late-stage development global project teams. Preferred: PhD/Pharm D or MS/MA/MPH with at least 10 years as a writing professional in pharmaceutical industry, with 2-5 years' experience in managing/supervising activities associated with the

As the Lead Medical Writer in our R&D clinical team, you will provide insights and expertise on regulatory gap closures and best practices as well as conduct clinical-related technical writing for medical device regulatory projects (CER, MDD/ MDR compliant format, literature review and analysis). Ge