Responsibilities *Help with the preparation and submission of applications of reliable quality in a timely manner to MHRA (UK) via National Procedure. These include new licence applications, variations (including grouping and work sharing), renewals, artwork changes, RFIs, updates and any other...

A start up pharmaceutical client is looking for a Regulatory Affairs Executive on a permanent basis. The role is focused on submitting applications via NP and the ideal candidate would be responsible for mentoring junior regulatory team members as well as liaising with relevant regulatory autho...

My client, a well established Oxford based Biopharma, currently seeks a CMC professional at Senior Manager / Associate Director level to join their team. Within this role you will be responsible for Global CMC and managing and leading registration and CMC regulatory support for commercial and ...

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...

An excellent opportunity has arisen for a Regulatory Associate to begin their Regulatory career within an exciting emerging pharmaceutical company based in Berkshire. The role of the regulatory affairs associate will be to support the team in the preparation and submission of applications, an...

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...

Within this role you will provide regional regulatory support for multiple products. It is essential that you have STRONG strategy and recent EMA clinical experience. You will have a strong background supporting the diversity of regulatory procedures in the EU (inc. PIPs, variations, IMPDs, ...

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 exciting opportunity has become available for an experienced and enthusiastic Regulatory Affairs Executive / Senior Regulatory Officer, to join an exciting new client based in Berkshire! The successful candidate will have a strong background in registration and post approval submissions, an...

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 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, a well established Oxford based Biopharma, currently seeks a CMC professional at Senior Manager / Associate Director level to join their team. Within this role you will be responsible for Global CMC and managing and leading registration and CMC regulatory support for commercial and ...

An exciting opportunity has become available for an experienced and enthusiastic Regulatory Affairs Executive / Senior Regulatory Officer, to join an exciting new client based in Berkshire! The successful candidate will have a strong background in registration and post approval submissions, an...

Within this role you will provide regional regulatory support for one or more products, and as a member of the EU Oncology Regulatory Team. You will have a strong background supporting the diversity of regulatory procedures in the EU (inc. PIPs, variations, IMPDs, MAAs) and ability to work au...

Public Affairs Manager Junior wanted for our Basel based client in the pharmaceutical sector. Your experience/skills: * University degree in Public Affairs, Law, Policy, Health Economics or Business with work experience * Practical knowledge in a PA-related business, government or non-gover...

The Publishing and Submissions System Manager will be responsible for participating as an active member in cross-functional business teams that support the identification, development, delivery and maintenance of technology projects and systems within Global Pharma Development Regulatory (PDR)....

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...

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 ...

Responsibilities: Strategy and Execution * Plans and manage regulatory submissions for products within the company portfolio in compliance with global filing plans and local regulatory requirements. * Implement product related regulatory strategies, Regulatory Affairs processes and activity ...

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 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,...

Within this role you will provide regional regulatory support for multiple products. It is essential that you have STRONG strategy and recent EMA clinical experience. You will have a strong background supporting the diversity of regulatory procedures in the EU (inc. PIPs, variations, IMPDs, ...

Top tier contract rates on offer with a leading global biopharmaceutical company. Long term prospects available with possibility for extension. I am looking for a Regulatory Consultant to join my client's team in Surrey on a 12-month contract basis. As one of the world's premier biopharmaceut...

A start up pharmaceutical client is looking for a Regulatory Affairs Executive on a permanent basis. The role is focused on submitting applications via NP and the ideal candidate would be responsible for mentoring junior regulatory team members as well as liaising with relevant regulatory autho...