REGULATORY AND CLINICAL PROJECT jobs in EUROPE ENGLAND, United Kingdom

Regulatory and Clinical Project Manager High Wycombe - Hybrid (up to two days a week working from home) Paying up...’ experience of working in Regulatory with Clinical experience, and you will also need a project management qualification too...

We are looking for an individual contributor with advanced knowledge acquired from several years of experience within regulatory affairs in a clinical... documents to support clinical trial submissions as well as independently provide regulatory support for more complex projects...

Job Title: CMC Regulatory Affairs Manager- Submission Excellence and Project Management Location: Macclesfield (UK... contributions to the regulatory submissions linked to medicinal products throughout the product lifecycle; including Clinical Trial...

TRANSLATION PROJECT MANAGER – REGULATORY SUBMISSIONS Working with the wider Project Management team, the Translation... Project Manager – Regulatory Submissions is responsible for coordinating and managing the full lifecycle of Regulatory...

in the Life sciences Language Services industry Experience in leading a team of Project Managers within Regulatory...The Associate Director – Regulatory Submissions is responsible to lead a worldwide Regulatory Submissions delivery team...

Senior Project Clinical Data Manager We have the pleasure of working with a fantastic early phase CRO based in London... and it really is a very positive place to work Due to their growth, they are now looking for a Senior Project Clinical Data...

Senior Project Clinical Data Manager We have the pleasure of working with a fantastic early phase CRO based in London... and it really is a very positive place to work Due to their growth, they are now looking for a Senior Project Clinical Data...

Senior Project Clinical Data Manager We have the pleasure of working with a fantastic early phase CRO based in London... and it really is a very positive place to work Due to their growth, they are now looking for a Senior Project Clinical Data...

Title: Clinical Project Manager Company: Ipsen Bioscience, Inc. Job Description: Clinical Project Manager (CPM... and share the progress of the project, and work effectively as a Team Lead, Manage and Drive the cross-functional Clinical...

Project Assistant to join our Clinical Safety team. This position will work on a team to accomplish tasks and projects... and grow your career even further, then this is the opportunity for you. Responsibilities Provide day to day project...

We have a great roles for a Global Clinical Project Managers in Central London. Our client has an extensive global... days/ week for team collaboration. If you have some Clinical Project Management experience, working with clients...

Reference Number: JO-2404-533971 Regulatory Coordinator Rate: Negotiable Job Type: Contract Location: Reading... Job Title: Regulatory Affairs Coordinator CTA, CTR (Consultant) Job Type: 12 Month Contract Location: Berkshire, UK – Hybrid...

regulatory submissions linked to medicinal products throughout the commercial lifecycle; including Clinical Trial Applications... to deliver the needs of both the AZ business and the customer. You will project manage global CMC regulatory submissions ensuring...

product claims/labeling, ensuring that the provided clinical and non-clinical data are consistent with the required regulatory...-functional product/project teams and provides regulatory advice. Manages work groups and provides direction. Provides day...

representative on Project teams. Skills and Competencies Capable of developing and implementing optimal regulatory strategy.... Job Description The CMC (Chemistry, Manufacturing, and Controls) Regulatory Affairs International Affiliate Team is seeking a motivated...

would be beneficial Project and people management experience in regulatory affairs Ability to work onsite in a hybrid set up in the...REACH regulatory manager needed with management experience in the UK chemicals industry Regulatory Manager (REACH...

development, regional regulatory experience, clinical trial submission, product registration, line extension and license... maintenance. Global regulatory experience is a plus. Global and integrated cross-functional view into pharmaceutical project...