Regulatory Documents Jobs in Stevenage

We are seeking an experienced professional with advanced medical writing expertise who can independently manage complex regulatory writing projects. This role demands a deep understanding of clinical trial designs statistical analysis interpretation and clinical document processes.We create a place...

Job DescriptionThe Regional Dossier Publisher (RDP) will work within the Global Regulatory Affairs and Clinical Safety (GRACS) organization in the EUEEMEA Regulatory Operations (RRO-EUEEMEA) Team.The RDP is responsible for publishing key regulatory submissions in the region and supporting the publis...

You will lead medical writing activities that support clinical development and regulatory submissions. You will work closely with clinical pharmacology non-clinical pre-clinical research regulatory biostatistics and/or external partners to plan author and deliver complex documents. We value clear sc...

Business IntroductionAt GSK we have bold ambitions for patients aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines combining our understanding of the immune system with cutting-edge technology to...

Director Oncology Translational Research Liaison ScienceJob PurposeThe Director Oncology Translational Research Liaison Science will play a key role in the Oncology Translational Research (OTR) team within GSK Oncology. The post holder will exploit GSK proprietary and internally generated datasets f...