A full- service, global medical communications agency has an exciting opportunity for an experienced Regulatory Writer to join their talented team in East Cheshire. The agency is open to full-time or part-time working, as well as some home-working. As the Senior Regulatory Writer you will prep...

Regulatory Affairs Specialist (m/w) in the northern part of Switzerland Our customer collaborates with healthcare professionals around the globe to advance the pace of innovation in of medical devices. The products and solutions help treat patients suffering from disorders of, or injuries t...

An excellent opportunity has arisen for a Regulatory Specialist / Manager to join a Belgium based generics' company on a permanent basis. It is essential that the successful applicant has experience registering and maintaining licences with the Belgium authorities and have fluent Flemmish, Fre...

An excellent opportunity has arisen for a Regulatory Specialist to join a leading global Medical Device company based in Hertfordshire. If you have a background within Regulatory Medical Devices, and are keen to gain Class III product exposure, this role will offer you excellent career progres...

An excellent opportunity has arisen to join a leading Generics company at a Principle Regulatory Officer level with line management responsibilities. Within this role you will be responsible for managing a team of 4 - 6 regulatory professionals and provide technical advice and oversee projects...

My client is a leading pharmaceutical company based in the centre of Paris and they specialise in the development of human and veterinary medicine. Within this role you will gain exposure to extensive clinical development programs in oncology and in inflammatory and neurodegenerative diseases,...

An excellent opportunity has arisen for a Head of Regulatory / Medical Writing to join a Paris based pharmaceutical company specialising in the discovery, development, and commercialisation of novel targeted therapies for treating cancer, chronic inflammatory diseases and neurological degenerat...

An excellent opportunity has arisen to join a leading Generics company at a Senior Regulatory Affairs Officer level. Within this role you will be responsible for managing EU registration and post approval activities as well as mentor junior staff and gain basic line management responsibilities...

An excellent opportunity has arisen to join a leading Pharmaceutical company at a Principle Regulatory Officer / Manager level. Within this role you will be responsible for managing a team of 4 - 6 regulatory professionals and provide technical advice and oversee projects for new and existing ...

My client, a well-established Pharmaceutical company based in Paris, currently seeks an experienced Regulatory Affairs Director to join their growing team and lead a major clinical development program in oncology, inflammatory and neurodegenerative diseases. The studies are ongoing in phase 3 ...

An excellent opportunity has arisen to join a leading Pharmaceutical company at a Principle Regulatory Officer / Manager level. Within this role you will be responsible for managing a team of 4 - 6 regulatory professionals and provide technical advice and oversee projects for new and existing ...

An excellent opportunity has arisen for a Regulatory Affairs Officer to join a Hertfordshire based client within their exciting and fast moving team. The ideal person will have a strong background in EU regulatory and with a minimum of 18 months of industry regulatory exposure. Responsibiliti...

An excellent opportunity has arisen for a Senior Regulatory Affairs Manager / Associate Director to join a leading Pharmaceutical company based in Buckinghamshire on a permanent basis. This role has become available due to a period of growth within the company and a number of employee's receiv...

My client is currently seeking a Regulatory Affairs CTA Submissions Manager to join their team on a 12 month contract basis. This position is responsible for managing regulatory Clinical Trial Applications (CTA) submission activities for assigned clinical trials (Phase 1 - Phase 4 spanning fiv...

An excellent opportunity has arisen for a Regulatory Affairs Officer to join a Hertfordshire based client within their exciting and fast moving team. The ideal person will have a strong background in EU regulatory and with a minimum of 1 years of industry regulatory exposure. Responsibilities...

An excellent opportunity has arisen for a Senior Regulatory Affairs Officer to join a Hertfordshire based client within their exciting and fast moving team. The ideal person will have a strong background in EU regulatory and with a minimum of 3 years of industry regulatory exposure. Responsib...

An excellent opportunity has arisen for a Regulatory Affairs Officer to join a Hertfordshire based client within their exciting and fast moving team. The ideal person will have a strong background in EU regulatory and with a minimum of 1 years of industry regulatory exposure. Responsibilities...

An excellent opportunity has arisen for a Regulatory Manager / Team Leader to join a global team within a specialist Pharmaceutical company based on the south coast. Within this role you will gain a large amount of exposure working closely with R&D, QA and PV teams and lead a team of Regulatory...

Registration Information Associate with profound Regulatory Affairs knowledge wanted for our Basel based client in the pharmaceutical sector. Your experience/skills: * University degree with practical knowledge in the pharmaceutical or similar sector from outside Europe or US * 3+ years' wo...

Regulatory Affairs Manager (m/f) Medical Devices Munich I am currently working on an exclusive basis with a fantastic company located in the Munich area. My client is a Global leader within the corner of the Medical Device market in which they are active, and offer the chance to broaden y...

Regulatory Affairs - Medical Devices m/f Munich My client located in the Munich area are a pioneer within the Medical Device industry with over 100 years operating in their area of the market. You will have the chance to join a dynamic, motivated group of professionals who all share the...

My client, a well-established Pharmaceutical company based in Paris, currently seeks an experienced Regulatory Affairs Director to join their growing team and lead a major clinical development program in oncology, inflammatory and neurodegenerative diseases. The studies are ongoing in phase 3 ...

My client is currently seeking a Regulatory Affairs CTA Submissions Manager to join their team on a 12 month contract basis. This position is responsible for managing regulatory Clinical Trial Applications (CTA) submission activities for assigned clinical trials (Phase 1 - Phase 4 spanning fiv...

An excellent opportunity has arisen for a Senior Regulatory Affairs Manager / Associate Director to join a leading Pharmaceutical company based in Buckinghamshire on a permanent basis. This role has become available due to a period of growth within the company and a number of employee's receiv...

Global Regulatory Affairs Manager with profound project management skills wanted for our Vevey based client Your experience/skills: * Doctorate in Sciences, Medicine or Pharmacy * Master or any equivalent advanced scientific degree in a related technical field * 3+ years' of work experienc...