REGULATORY AND CLINICAL PROJECT jobs in United Kingdom #2

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...

SRG

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...

UCB

intelligence expertise, regulatory affairs, pre-clinical, clinical, and commercial areas for investigational and marketed products... is desired. Follow regulatory plans and interface with project team members, both within the organization...

CooperVision

regulatory strategy(s) and for delivery of clinical trial applications and approvals according to plans. The role requires... EMA. You will work with the Clinical Development Team and with the global regulatory and regional leads, to ensure...

GlaxoSmithKline

Overview As a Regulatory Publishing Specialist you will be joining the world’s largest & most comprehensive clinical... compilation of granular clinical study reports and other regulatory documents Performs document formatting reviews...

ICON

on pre-clinical and clinical development plans and work with both Regulatory Affairs – New Products and Regulatory Affairs... (for study adequacy, and data presentation, risk analysis), leading or supporting any regulatory interaction on Clinical...

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...

Zest Scientific

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...

Gilead

on our business. About the Role: As a Regulatory Affairs Manager, you will play a pivotal role in leading a team of Project... of Project Managers and Regulatory Affairs Specialists focused on the UK market. Managing all regulatory activities relating...

AbbVie

Expert on the regulatory environment and intelligence within the UK and Ireland and contributes to preparing new local... regulatory guidance documents when applicable. Managed initial marketing authorization (MA) applications, variations...

Actalent

Specific Job Requirements Expert on the regulatory environment and intelligence within the UK and Ireland... and contributes to preparing new local regulatory guidance documents when applicable. Managed initial marketing authorization...

Actalent

Specific Job Requirements Expert on the regulatory environment and intelligence within the UK and Ireland... and contributes to preparing new local regulatory guidance documents when applicable. Managed initial marketing authorization...

Actalent

Reporting to the Head of Clinical & Regulatory Affairs, the Regulatory Affairs Manager will be responsible... and International Regulatory requirements, effectively communicating to management and where required, project teams. Responsible...

eakin

lives. Read more: The European Regulatory Procedural Strategist (ERPS) team leads and manages the procedural... and operational aspects of the European regulatory filings within the European Centralised Procedure, working in close collaboration...

Bristol-Myers Squibb

regional regulatory strategy, including clinical trial application submissions and the affiliate commercial strategy...Salary: £400 - £500 per hour Job type: Contract * Discipline: Project Manager * Location: United Kingdom City...

Proclinical

of product development from clinical to lifecycle. Support may include organizing, managing and executing on regulatory CMC...CK Group are recruiting for a Regulatory Affairs Associate to join a biopharmaceutical company who are based in...

CK Group

. For new clinical trial and regulatory project proposals and ongoing projects, provide regulatory intelligence in support..., you will lead the efforts to gather, analyze, and disseminate regulatory information and intelligence that impacts Rho’s project...

Rho