REGULATORY CLINICAL STRATEGY SUBMISSIONS jobs in LONDON, United Kingdom

and compliant submissions and approvals. Advise senior management on regulatory and clinical strategy pathways and options... with regulatory registration strategy. Support the build of global clinical development strategy based on correct interpretation...

Job Description Join our team as a Clinical Quality Operations Lead - Inspection Strategy and be at the forefront... and guidance will ensure the smooth management, training, and support of regulatory Health Authority inspections, solidifying...

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...

and manage regulatory submissions (e.g. clinical trial and marketing applications) for products within the client's portfolio... and/or support staff. Responsible for: Advising the Global Regulatory Team on regional considerations in developing strategy...

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...

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...

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...

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...

as local HA liaison (e.g., FDA or EMA). Regulatory Submissions Leads planning, preparation and submission of clinical... regulatory strategy for program(s) through development, registration and post approval in the assigned region(s). They may act...

, product specialists, marketing, regulatory and medical, and inputs as required with key wording and collation of clinical... is to educate and support both HCPs and internal teams on clinical aspects of Ostomy care. To support with education from diagnosis...

regulatory leads (GRL) and UK cross functional stakeholders, advise on clinical trial strategy... This is what you will do: This position is responsible for development and implementation of the UK and Ireland regulatory strategy and activities...

submissions that meet rigorous regulatory standards. With a global footprint across four continents, MMS maintains a 97 percent... with a proven, scientific approach to complex trial data and regulatory submission challenges. Strong industry experience...

strategy, resolving project related issues where required. Ensure collaboration across Regulatory & Site Activation, including... business development, initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements...

for marketing and clinical trial submissions. Additionally, they coordinate timelines, virtual documents, and the generation of the... developing the technical eCTD sections to support Regulatory CMC dossier applications. They work with limited guidance from the...

. Knowledge of and experience in selling biometrics, regulatory submissions, and regulatory operations will be a distinct... industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint...

. Knowledge of and experience in selling biometrics, regulatory submissions, and regulatory operations will be a distinct... industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint...