Who we are For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance
Safety Physician – Director Level Global Development | Rare Disease & Neurology | UK You are a medically trained safety leader who wants to move beyond execution and play a defining role in how development programmes
We are looking for experienced Freelance Medical Writers to support an immediate requirement with a leading international organisation working within the life sciences industry. This opportunity would suit an experienced clinical/regulatory writer who has current availability
ROLE OVERVIEW We are currently looking for a Director of Formulation & Process Development to join a leading pharmaceutical contract development and manufacturing organisation based in Northern Ireland. This is an exciting opportunity for an experienced
Head of Regulatory Affairs Location: Flexible / Hybrid Travel: Frequent international travel required Lead Global Regulatory Strategy for Innovative Medical Technologies Corin is seeking an experienced and strategic Head of Regulatory Affairs to lead our Global
The Clinical Unit Cambridge (CUC) is GSK’s MHRA-accredited early-phase clinical and translational medicine centre, combining Phase I clinical trial delivery, advanced translational science, biomarker discovery, single-cell and spatial omics capabilities, and technology-enabled operations to generate high-quality