REGULATORY AND CLINICAL PROJECT jobs in EUROPE ENGLAND, United Kingdom #2

at least one of the following areas: clinical data disclosure/transparency, regulatory affairs, clinical operations, or consulting for R.... · Well-versed in preparing or reviewing clinical and/or regulatory documents and/or experience in summarizing scientific information...

of regulatory health authority interactions, inspections and/or external advocacy/regulatory policy Customer & Project management...CMC Regulatory Affairs Director, Device Submissions Lead Location: Macclesfield (UK) Are you passionate about the...

Director, Regulatory Medical Writing, Oncology At Johnson & Johnson, we believe health is everything. Our strength in... hypertension, and retinal disease. We are recruiting for a Director to join the Regulatory Medical Writing team to support the...

Director, Regulatory Medical Writing, Oncology At Johnson & Johnson, we believe health is everything. Our strength in..., and retinal disease. We are recruiting for a Director to join the Regulatory Medical Writing team to support the Oncology...

(s) Chairs a Global Regulatory Team (GRT) of regulatory Subject Matter Expert(s) Provides global regulatory leadership... of assigned program(s) Develops global regulatory strategies, including risk assessment and mitigation strategies. Champions...

within area of responsibility. Represents Regulatory Affairs on cross-functional product/project teams and provides regulatory...Description Senior Manager Regulatory Affairs (Regional Skin Health) Located: High Wycombe, UK (Hybrid) Who...

, or Germany. Responsibilities: – Write and/or edit various clinical regulatory documents: As a Senior Regulatory Affairs... Writer, you will be responsible for writing and editing a wide range of clinical regulatory documents, including CSRs, IBs...

industry's most innovative clinical stage biotechnology companies, this is a fantastic opportunity to provide expert regulatory..., supplements, variations and other communications with regulatory authorities. · Attend project team meetings and provide CMC...

activities of this Partner encompass: Support the team in ensuring that regulatory requirements are met for Clinical Trial... structure across the UK Affiliate Provide regulatory advice to project teams (e.g.: Squads, Work Packages, etc) to ensure...

industry's most innovative clinical stage biotechnology companies, this is a fantastic opportunity to provide expert regulatory... of project teams and responsible for developing regulatory strategy across the company. You will be responsible for ensuring the...

Reporting to the Head of Regulatory Affairs you will collaborate and develop the Regulatory and Quality strategy... for the UK. This role is responsible for the execution in delivery of the regulatory milestones including assessment of the...

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...

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...

and comprehensive expertise within the Regulatory environment you will lead project work and partner with the business to solve complex...: Support the team in ensuring that regulatory requirements are met for Clinical Trial Applications that involve Medical Devices...

Teams or other Regulatory Project Teams and represent Global TA Regulatory on cross-functional core and sub-teams. In... Teams or other Regulatory Project Teams and represent Global TA Regulatory on cross-functional core and sub-teams...