Regulatory affairs associate jobs in Egham

CK Group are recruiting for a Regulatory Affairs Associate to join a biopharmaceutical company who are based in Uxbridge on a contract basis for 12 months. Company: Our client is committed to ...

CK Group are recruiting for a Senior Manager Regulatory Affairs to join a biopharmaceutical company who are based in Uxbridge or Cambridge on a contract basis for 12 months. Company: Our client is ...

Regulatory Affairs Associate Location: Maidenhead / M4 corridor. Salary: Very competitive salary on offer Planet Pharma are supporting a leading large global pharma company with the search for a new ...

Associate Regulatory Affairs Type: Contract Length: 12 Months Location: London We've currently partnered with a global pharma who are looking for a Associate regulatory affairs CMC in their London ...

Regulatory Affairs - Clinical Trial Services - Hybrid Opportunity Are you ready to advance your career with a leader in Clinical Services? Providing the opportunity to specialise in a niche area of a ...

Regulatory Affairs Coordinator CTA/CTR (Consultant) Job Type: 12 Month Contract Location: Berkshire, UK - 2 days on site per week Rate: Up to £55 per hour PAYE (inside IR35) We are partnered with a ...

CK Group are recruiting for a Regulatory Affairs Associate to join a biopharmaceutical company who are based in Uxbridge on a contract basis for 12 months. Regulatory Affairs Associate Role:. Experience in a Regulatory Affairs role in CMC, including preparation of submissions to Agencies and fami...

Associate Director Regulatory Affairs. Works with the Lead, Regulatory Affairs, and the Development Team, and with moderate/minimal supervision, with select project teams within subsidiary organizations to develop and oversee program-specific regulatory, clinical, and development strategies. Resp...

Planet Pharma are supporting a leading large global pharma company with the search for a new Regulatory Affairs Associate to join them during an exciting period of growth! Perfect for a junior regulatory professional with 6-24 months regulatory experience!. Manage the operational and technical as...

Our client, a global pharmaceutical company, is currently looking for a CMC Regulatory Affairs Associate to join their team in Uxbridge. ...

As Associate Director, Global Regulatory Affairs Strategy, you will be responsible for:. To be considered as the Associate Director, Global Regulatory Affairs Strategy, you will have the following:. Understand the regulatory landscape, assess regulatory risks, and develop global filing strategies...

Planet Pharma are supporting a leading large global pharma company with the search for a new Regulatory Affairs Associate to join them during an exciting period of growth! Perfect for a junior regulatory professional with 6-24 months regulatory experience!. Manage the operational and technical as...

Extensive experience in Regulatory Affairs with experience acting as therapeutic area European Regulatory Affairs lead, defining and implement regulatory strategies and executional plans. Define and advise the GRT on regional considerations in developing creative regulatory strategy, lead develop...

Associate Director - Quantity Surveying. ...

Zest Scientific is actively recruiting for a Senior Regulatory Specialist in the field of medical devices for a leading global drug development organization. With broad and comprehensive expertise within the Regulatory environment you will lead project work and partner with the business to solve ...

As a Regulatory Publishing Specialist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. As a Regulatory Publishing Specialist you will be fully dedicated to a Top-5 pharmaceutical company. PDF files intended for regula...

Senior Regulatory Affairs Specialist to work at Corin, you will be responsible for product registration and all regulatory aspects of post-market surveillance. The Senior Regulatory Affairs Specialist will require extensive knowledge of all applicable standards, regulations, and guidance to suppo...

Expertise in authoring and reviewing of regulatory documents; development regulatory documents; Regulatory Strategy Plans, Clinical and Drug Development Plans, Clinical Trial Applications, Pre-INDs, INDs, Scientific Advice and Meeting Briefing Documents, Orphan Drug and Paediatric plans/applicati...

You will be an experienced medical writer who has worked for medical communications/market access consulting firms for several years, ideally with some people leadership/mentoring experience. New: Senior Medical Writer - Market Access / Value Communications / HEOR. A secure and steady flow of lon...

Regulatory affairs CMC Consultant. Ensure that the content of CMC work-packages and documentation are phase appropriate, meet regulatory expectations and enable approval of regulatory submissions. At least five years in a scientific/technical CMC development or CMC – regulatory affairs function. ...

As a Project Manager, you will be responsible for managing all aspects of a large-scale development project, involving both educational facilities and residential housing. We are a leading construction and project management firm dedicated to delivering outstanding development projects across var...

Assist the Head of Compliance in all areas of compliance including preparing for any regulatory changes, ongoing monitoring and any ad hoc compliance projects. Senior Compliance Officer (Contract). Very successful and established stock broking and wealth management company have a generalist compl...

Regulatory Affairs Advisor (Arabic Speaking). At Campden BRI, we have a dedicated Regulatory Affairs Team who offer a valuable and expert advisory service, as we're the leading authority, helping our clients stay compliant with food regulations in more than 80 countries! We are widely recognised ...

Publications, medical communications, medical education, congress activities. If you’re an experienced writer, seeking to join a team of strong writers and have mentoring responsibilities, this could be a great fit! We’re looking for someone who has:. At least 3 years of experience working as a w...