Global Regulatory Strategy Lead

Job SummaryWe are seeking a highly skilled Regulatory Affairs Director to lead our global virology regulatory efforts. This individual will be responsible for defining the regulatory strategy for multiple products or projects, overseeing the preparation and maintenance of regulatory submissions, and representing Gilead in negotiations with regulatory...

Job Summary:A seasoned Regulatory Affairs Senior Manager is required by a prominent pharmaceutical company in Uxbridge. The successful candidate will be responsible for developing and implementing regulatory strategies across various products, ensuring alignment with global regulations and the company's business model.This role involves collaborating with...

Lifelancer offers a unique opportunity for a talented professional to join our team as a Global Regulatory Sciences Director. This role is an excellent fit for individuals who are passionate about transforming patients' lives through science.As a Global Regulatory Sciences Director at Lifelancer, you will be responsible for leading the development of...

PE Global are currently recruiting for a Sr Manager Regulatory Affairs (CTA) for an initial 12 month contract role with a leading multinational Pharma client based in either Uxbridge or Cambridge - hybrid.To ensure that our client acquires and maintains all the required licenses in order to support clinical trials for investigational medicinal products as...

PE Global are currently recruiting for a Sr Manager Regulatory Affairs (CTA) for an initial 12 month contract role with a leading multinational Pharma client based in either Uxbridge or Cambridge - hybrid.To ensure that our client acquires and maintains all the required licenses in order to support clinical trials for investigational medicinal products as...

PE Global are currently recruiting for a Sr Manager Regulatory Affairs (CTA) for an initial 12 month contract role with a leading multinational Pharma client based in either Uxbridge or Cambridge - hybrid.To ensure that our client acquires and maintains all the required licenses in order to support clinical trials for investigational medicinal products as...

Job Description PE Global are currently recruiting for a Sr Manager Regulatory Affairs (CTA) for an initial 12 month contract role with a leading multinational Pharma client based in either Uxbridge or Cambridge - hybrid. To ensure that our client acquires and maintains all the required licenses in order to support clinical trials for investigational...

PE Global are currently recruiting for a Sr Manager Regulatory Affairs (CTA) for an initial 12 month contract role with a leading multinational Pharma client based in either Uxbridge or Cambridge - hybrid.To ensure that our client acquires and maintains all the required licenses in order to support clinical trials for investigational medicinal products as...

PE Global are currently recruiting for a Sr Manager Regulatory Affairs (CTA) for an initial 12 month contract role with a leading multinational Pharma client based in either Uxbridge or Cambridge - hybrid. To ensure that our client acquires and maintains all the required licenses in order to support clinical trials for investigational medicinal products as...

Job Description:A Senior Regulatory Affairs Manager is required by a global pharmaceutical company based in Uxbridge. The successful candidate will be responsible for developing and defining regulatory plans across multiple products.This is an exciting opportunity to work with a team who are passionate about delivering excellence and focused on sharing...

Job Summary:We are looking for a Senior Regulatory Affairs Manager to join our client's team in Uxbridge. The role involves developing and implementing regulatory strategies to ensure compliance with global regulatory requirements.The ideal candidate will have experience as a Regulatory Lead managing at least 1 product end to end lifecycle and be able to...

About the Role">As a Senior Regulatory Affairs Manager, you will be responsible for providing centralised regulatory strategy and guidance across the region.Your key responsibilities will include:">Developing and contributing to high-quality regulatory documents needed to support clinical trials and medical products.Providing regulatory guidance to enhance...

**Job Description**Gilead Sciences, Inc. is a leading biopharmaceutical company that seeks an experienced Regulatory Affairs professional to join its team as an Associate Director, Global TA Regulatory Liaisons, Virology. This role will oversee the preparation and maintenance of regulatory submissions, labeling, and packaging for assigned products or...

About the Role:We are seeking an experienced Regulatory Affairs Senior Manager to join our team in Uxbridge. In this role, you will develop and execute regulatory strategies to ensure compliance with global regulations and our business model. You will collaborate with cross-functional teams to provide regulatory guidance, contribute to product development,...

We are seeking experienced Regulatory Affairs professionals to join our dynamic team in support of a global acceleration client initiative for late-stage phase III assets.About the RoleThis is an exciting opportunity to play a crucial role in accelerating time to filing and approval in Global Country Initiative (GCI), emerging markets, and non-EU markets.Key...

Role OverviewPark Street People is currently looking for a Senior Regulatory Affairs Manager to join their team in Uxbridge. The ideal candidate will be a confident Regulatory Lead with experience in developing and defining regulatory plans across multiple products.The role involves working closely with the regulatory team and stakeholders to provide...

PE Global are currently recruiting for a Sr Manager Regulatory Affairs (CTA) for an initial 12 month contract role with a leading multinational Pharma client based in either Uxbridge or Cambridge - hybrid.To ensure that our client acquires and maintains all the required licenses in order to support clinical trials for investigational medicinal products as...

**Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...

Job SummaryWe are seeking a highly experienced Regulatory Affairs specialist to join our team in support of a global acceleration client initiative. This exciting opportunity will see you play a crucial role in accelerating time to filing and approval in various markets.About the RoleThis is an excellent chance to work with a dynamic team on a mission to...

PE Global are currently recruiting for a Sr Manager Regulatory Affairs (CTA) for an initial 12 month contract role with a leading multinational Pharma client based in either Uxbridge or Cambridge - hybrid. To ensure that our client acquires and maintains all the required licenses in order to support clinical trials for investigational medicinal products as...