CLINICAL AND REGULATORY PRODUCT jobs in CAMBRIDGE, United Kingdom

for Gilead’s growing oncology development product portfolio, allowing you to strengthen your drug development and regulatory... for a Regulatory Affairs Associate Director to join the Gilead Global Regulatory Affairs Oncology team to support drug development...

. You will maintain awareness of regulatory intelligence and guidance, as this impacts product labeling, artwork, and translations... regulatory submissions, such as Closing Sequences, and ensuring product packaging and associated information...

innovative medical devices, which we use in clinical trials to collect a biobank of mucus-based biospecimens. This biobank... provides clinical material for our research and development streams to assist with diagnostic development. Our primary...

and strategic commercial launch planning Experience with US and EU regulatory filings for both clinical trial and marketing...Job Purpose The Clinical Supply Chain Manager is responsible for coordination of all supply matters for clinical...

Job Purpose The Clinical Science Specialist will provide appropriate leadership and management within Clinical... Development, to provide scientific and clinical development support for products within MoonLake Immunotherapeutics assigned...

experience in the biopharma industry, regulatory agency, clinical research or other related healthcare environment, including... into product development and lifecycle management as well as perform or oversee other advanced MSS activities...

markets where they trade in. Scope of Work/Objectives Working closely with the own brand clinical expert, agree a product..., We are looking for an experienced own brand expert to develop the own brand proposition, find best sources and develop a sourcing and product roadmap...

appreciation of the regulatory requirements for a clinical laboratory (ISO 15189) and IVD, ISO 13485 Good written and verbal...Temporary Senior QC Scientist - Clinical Laboratory Cambridge 11 week assignment beginning early July Monday...

of a busy clinical laboratory. Core duties: Working within quality control matrix and protocols to ensure the smooth... operation of both routine QC and unique QC testing for the company's IVD product, as well as continuous improvement behaviours...

clinical safety assessments and regulatory reports/submissions involving safety information. Experience working with vendor... and risk management activities for MoonLake products in clinical development. The role actively contributes to setting the...

the clinical and health economic value of some of the newest and most innovative therapies in development Salary... the division you will work on the successful delivery of projects to demonstrate the clinical and health economic value...

Role summary Responsibilities: You will work on the successful delivery of projects to demonstrate the clinical... to demonstrate the clinical and health economic value of some of the newest and most innovative therapies in development. In...

possible, together. Job Description Description: Serves as a senior scientific and clinical expert for safety profile of products... in therapeutic areas Defines global product safety strategy and routinely manages and leads functional and cross...

all clinical phases, with demonstrable experience in a GCP quality/compliance role Knowledge of GCP, FDA, MHRA and EMA regulatory... understanding of global drug development functional areas including preclinical, clinical, regulatory affairs and manufacturing...

Strategy, Regulatory Operations & Market Access, CMC & Quality, Non-Clinical and Clinical Development Strategy. Collaborating... global expert teams dedicated to providing comprehensive global regulatory consulting services in the areas of Regulatory...

global regulatory consulting services in the areas of Regulatory Strategy, Regulatory Operations & Market Access, CMC... & Quality, Non-Clinical and Clinical Development Strategy. Collaborating with senior management, you will contribute to the...

’s clinical and commercial products and is responsible for always keeping the internal and external manufacturing processes in...). GCSAT is responsible for optimization and life cycle management of Sobis clinical and commercial manufacturing processes...