REGULATORY AND CLINICAL PROJECT jobs in SOUTH EAST ENGLAND EAST, 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...

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...

. Clinicology offers a full range of services including site start-up, monitoring, project management, regulatory submissions... of assigned clinical trials, including contract and financial invoicing. Ensure project deliverables...

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...

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...

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...

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...

Manager, Regulatory Medical Writing - Immunology At Johnson & Johnson, we believe health is everything. Our strength... of tomorrow, and profoundly impact health for humanity. Learn more at We are recruiting for a Manager, Regulatory Medical Writing, located in...

to, clinical study reports, investigator's brochures, study protocols, summary documents, risk management plans, regulatory...Manager Regulatory Medical Writing, Oncology At Johnson & Johnson Innovative Medicine, what matters most is helping...

regulatory requirements are met for Clinical Trial Applications involving Medical Devices. Monitor changes to the UK Regulatory... and adaptation of the medical device structure across the UK Affiliate. Provide regulatory advice to project teams to ensure...

advice to project teams to ensure continued regulatory compliance and timely market release. Support external regulatory...CK Group are recruiting for a Regulatory Partner (Medical Devices) to join a company in the Pharmaceutical industry...

that regulatory requirements are met for Clinical Trial Applications that involve Medical Devices of any nature (e.g. physical devices... regulatory advice to project teams to ensure continued regulatory compliance and timely market release. Support external...

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...

approval, regulatory affairs, drug development consultancy, and post approval/marketing support. We are known for our hands...-on problem-solving approach and enjoy tackling the unique challenges that each project brings. Our clients span the...

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...

with relevant regulatory framework Create and maintain demand forecasts and packaging plans so that packed clinical supplies... experience in Clinical Supply Chain Management (Essential). 2-3 Years with IRT systems Ability to demonstrate good project...