Global Maintenance Regulatory Manager wanted for our Basel based client in the pharmaceutical sector. Your experience/skills: * University Degree, preferred PhD in the following sections like Life Sciences, Pharmacy or Medicine * 2+ years' work experience in related areas of the pharma Ind...

My client, an international biopharmaceutical company focussing within sleep and haematology/oncology, is currently searching for a Regulatory Affairs Director to join their team based in Oxfordshire. As the Regulatory Director, you will be key stakeholder in the company's regulatory activiti...

Within this role you will provide regional regulatory support for one or more products, and as a member of the Global Regulatory Team (GRT), will be accountable for developing and executing regional regulatory strategies across the product lifecycle and managing effective agency interactions. ...

Within this role you will assist with, under the direction of a Regional Regulatory Lead, the creation and submission of regulatory documents and you may be the regulatory lead for a program under the supervision of a more experienced regulatory lead! Responsibilities: -Assist Regional Regul...

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,...

My client, an established Biopharma based in Oxfordshire is currently searching for an experienced Regulatory Affairs Manager to join their Labeling labelling team on initial 6-12 month contract basis. Within this role you will be responsible for regulatory support (both technical and operation...

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 for a Senior Regulatory Officer 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. The ideal candidate will have a ...

An excellent opportunity has arisen for an experienced Regulatory Consultant, with a strong background in RoW and European strategy. The main focus of this role with be within post approval, but a candidate with development exposure would be preferable. Responsibilities: *You will participa...

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...

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,...

A excellent opportunity has arisen for a Regulatory affairs officer to join a specialist pharmaceutical company based in West Sussex. Within this role you will be responsible for performing & reviewing regulatory affairs activities, including the maintenance of New Product Registrations and th...

The client, based in Oxford, is looking for a RIM Consultant on a contract basis for 12 months initially. Within the role, the candidate would provide Global Regulatory Affairs Operations support for the Veeva Vault RIM system.The ideal candidate would be working with project team to update RIM...

An excellent opportunity has arisen for an experienced Regulatory Consultant, with a strong background in RoW and European strategy. The main focus of this role with be within post approval, but a candidate with development exposure would be preferable. Responsibilities: *You will participa...

Within this role you will assist with, under the direction of a Regional Regulatory Lead, the creation and submission of regulatory documents and you may be the regulatory lead for a program under the supervision of a more experienced regulatory lead! Responsibilities: -Assist Regional Regul...

Within this role you will provide regional regulatory support for one or more products, and as a member of the Global Regulatory Team (GRT), will be accountable for developing and executing regional regulatory strategies across the product lifecycle and managing effective agency interactions. ...

My client, an international biopharmaceutical company focussing within sleep and haematology/oncology, is currently searching for a Regulatory Affairs Director to join their team based in Oxfordshire. As the Regulatory Director, you will be key stakeholder in the company's regulatory activiti...

My client, an established Biopharma based in Oxfordshire is currently searching for an experienced Regulatory Affairs Manager to join their Labeling labelling team on initial 6-12 month contract basis. Within this role you will be responsible for regulatory support (both technical and operation...

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,...

A excellent opportunity has arisen for a Regulatory affairs officer to join a specialist pharmaceutical company based in West Sussex. Within this role you will be responsible for performing & reviewing regulatory affairs activities, including the maintenance of New Product Registrations and th...

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...

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 Senior Regulatory Officer 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. The ideal candidate will have a ...

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 ...

Within this role you will provide regional regulatory support for one or more products, and as a member of the Global Regulatory Team (GRT), will be accountable for developing and executing regional regulatory strategies across the product lifecycle and managing effective agency interactions. ...