REGULATORY AND CLINICAL PROJECT jobs in HOME COUNTIES, 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...

Harris Lord

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...

IQVIA

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...

IQVIA

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...

Clinical Professionals

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...

Johnson & Johnson

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

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

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

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

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...

Johnson & Johnson

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...

CK Group

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...

CK Group

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...

TMC

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...

IQVIA

Provide scientifically rigorous statistical input into project development plans, regulatory submissions and questions... of deliverables according to project plans. Develop effective collaborations with others within clinical teams, partner lines...

to support our clinical research team on a project basis. The successful candidate will be responsible for drafting clear..., concise, and compliant clinical trial protocols in accordance with regulatory guidelines and industry best practices...

Ellison Institute of Technology

team on a project by project basis. The successful candidate will play a crucial role in securing funding for clinical... brochures, and protocols. Strong understanding of clinical trial design and methodologies, and regulatory requirements...

Ellison Institute of Technology