REGULATORY AFFAIRS MANAGER IN jobs in CAMBRIDGESHIRE, United Kingdom

Job title: Senior Manager Regulatory Affairs Writing A growing Biotech in Cambridge with multiple Phase 3 assets... are seeking a Senior Manager Regulatory Affairs Writing. The role will play a...

Pharma Partners

Job title: Senior Regulatory Affairs Manager CMC A growing Biotech in Cambridge with multiple Phase 3 assets... are seeking a Senior Regulatory Affairs Manager CMC. The role will be responsible...

Pharma Partners

experts in Europe. The business is currently looking for a Regulatory Affairs Manager to join the business and take the lead...Reference Number: JO-2404-532760 Regulatory Affairs Manager Rate: £50,000 – 55,000 Job Type: Permanent Location...

Clinical Professionals

/BS with 8+ years relevant experience Previous experience in multiple aspects of Regulatory Affairs including partnering... possible, together. Job Description Regulatory Affairs Vendor Governance is a function within the RA Business Operations group...

Gilead

Origin Sciences is a start-up biotechnology company based in Granta Park, just south of Cambridge. We develop our own... innovative medical devices, which we use in clinical trials to collect a biobank of mucus-based biospecimens. This biobank...

Origin Sciences

Job Purpose The Senior Manager, Medical & Regulatory Writing will be an integral part of MoonLake’s Clinical... and other controlled documents, including for Medical and Regulatory writing activities Partners with Regulatory Affairs and cross...

MoonLake Immunotherapeutics

Job Purpose The Manager, Medical & Regulatory Writing will be an integral part of MoonLake’s Clinical Development... Partners with Regulatory Affairs and cross-functional colleagues to understand the clinical development landscape e.g...

MoonLake Immunotherapeutics

Job Purpose As a Senior Manager, Regulatory Affairs CMC, you are an integral part of MoonLake’s Clinical Development... Senior Manager, Regulatory Affairs CMC will serve as a subject matter expert, which will involve collaborating with multiple...

MoonLake Immunotherapeutics

of regulatory affairs in achieving cross-functional drug discovery, development, and commercial goals and objectives, including... in associated regulatory submissions. You will represent RO LAT on Regulatory Project Teams, in cross-functional...

Gilead

deviations) Work closely with CRA’s and research scientists. Interface with Program Management, Clinical Affairs, Regulatory...Job Title Clinical Operations Manager – Clinical Data Intelligence (Cambridge, MA) Job Description Clinical...

Philips

with existing policies and procedures, ICH GCP and applicable global regulatory requirements Participate in the planning, conduct... all clinical phases, with demonstrable experience in a GCP quality/compliance role Knowledge of GCP, FDA, MHRA and EMA regulatory...

Bicycle Therapeutics

would also be highly advantageous if you have a good understanding of Regulatory Affairs. Part of your role will involve working...A growing Medical Devices company based in Cambridge is currently looking for a new Quality Assurance Specialist...

Newton Colmore Consulting

, Robotics, Science, Electronics Design, New Product Design, Human Factors, Regulatory Affairs, Quality Assurance and Field...A growing medical devices company, based in Cambridgeshire, are currently looking to add a design engineer to the...

Newton Colmore Consulting

Product Design, Human Factors, Regulatory Affairs, Quality Assurance and Field Service Engineering sectors. Manufacturing... sector, due to this they need a number of experienced embedded software engineers to be based in the Cambridgeshire labs...

Newton Colmore Consulting