REGULATORY CLINICAL STRATEGY SUBMISSIONS jobs in United Kingdom

Manager is accountable for submissions execution for designated CTAs. You will operate as regulatory operational Subject... and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services...

ICON

Location: Central London / West End Job Title: Senior Regulatory Labelling Consultant (Labelling Strategy) Location: UK... coordination, clinical supplies/packaging, supply chain regulatory affairs, or quality. Good working knowledge of key labeling...

Clinical Professionals

you will be responsible for building strategy, determining regulatory requirements and managing product license registrations with global... and compiling regulatory documentation, coordinating and executing regulatory submissions in compliance with ISO13485, IVD 2017/746...

Clinical Professionals

regulatory strategy, determining applicable regulatory requirements, proposing solutions to comply with regulatory requirements...Reference Number: JO-2403-531737 Senior Regulatory Associate Rate: Negotiable Job Type: Permanent Location...

Clinical Professionals

regulatory submissions, driving regulatory strategy, new registrations, and variations applications for a range of different... products including submitting submissions through National MRP and DCP. · Drive/support European regulatory strategies...

Clinical Professionals

Managers and Regulatory Director you will be responsible for generating regulatory submissions to target markets throughout... of regulatory applications (generally DCP, MRP,CP or national submissions) including responses to requests for further information...

Clinical Professionals

Reference Number: JO-2402-529333 Regulatory Affairs Lead/Head of Department Rate: Negotiable Job Type: Permanent... Location: Leamington Spa Regulatory Affairs Lead/Head of Department Leamington Spa, UK An opportunity to work...

Clinical Professionals

Job Purpose As a Senior Manager, Regulatory Affairs CMC, you are an integral part of MoonLake’s Clinical Development.... You will be responsible for the development of a CMC and device regulatory strategy, working closely with Technical Operations colleagues. The...

MoonLake Immunotherapeutics

European regulatory affairs experience (must have) Experience in Clinical Trial Applications in the EU (must have) Innovative... for a Senior Manager - Regulatory Affairs to work within the Global Regulatory Affairs - Innovative Medicines (Europe) team...

Teva Pharmaceuticals

on pre-clinical and clinical development plans and work with both Regulatory Affairs New Products and Regulatory Affairs... most efficient way. This will encompass Regulatory strategy planning, supporting due diligence assessment for any innovative assets...

Lifelancer

Quality and Regulatory Team and provide guidance to project teams on regulatory strategy and planning, quality system... design regulatory processes to join our team and work with project groups to translate novel technologies to the clinic...

King's College London

experience Experience in preparing regulatory submissions Experience in working with early-stage companies, where requirements...We are seeking experts in medical device design regulatory processes to join our team and work with project groups...

King's College London

experience Experience in preparing regulatory submissions Experience in working with early-stage companies, where requirements.... About us We are seeking experts in medical device design regulatory processes to join our team and work with project groups to translate novel...

King's College London

, Switzerland, and the UK. In this role you will need to provide provide regulatory strategy, leadership, and operational support... strategy for development or marketed products, taking in consideration the latest precedent, regulatory intelligence, agency...

Gilead

for assigned due diligences, under the direction of the Global Regulatory Strategy Lead? If so, our Biotechnology client...), paediatric plans, clinical trial designs and HA feedback. Accountable, with the GRSL, for providing a regulatory recommendation...

Randstad

. In this vital role you will provide regulatory strategy for lifecycle management synthetics (Small Molecule) products... across programs. Provide CMC regulatory strategy for assigned projects by defining minimal regulatory filing requirements...

Amgen

regulatory strategy for their assigned projects in the Vaccines and Infectious Disease therapeutic area. The selected... Agencies and/or subsidiaries with regard to global regulatory strategy/registration requirements for one or more of our Company...

MSD