Global Pharmaceutical Regulatory Manager

Global Regulatory Sciences Lead OpportunityAt Bristol-Myers Squibb, we're transforming the lives of patients and the careers of those who do it. This role offers the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity.Key ResponsibilitiesLead global regulatory strategy to support the...

Candidates for the Pharmaceutical Industry Regulatory Expert role will lead the procedural and operational aspects of European regulatory filings within the Centralised Procedure. This includes planning and tracking activities, communicating regulatory information, and providing logistical support for meetings.What You'll Do:Develop and implement strategies...

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...

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...

**Job Summary**Gilead Sciences, Inc. is a biopharmaceutical company that develops life-changing scientific innovations. We are seeking an experienced Regulatory Affairs professional to join our team as an Associate Director, Global TA Regulatory Liaisons, Virology.This role requires a deep understanding of European Medicines Agency (EMA) regulations and...

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...

About the RoleWe are seeking a talented Regulatory Management Specialist to join our team at Regeneron. This role will involve supporting the engagement of key stakeholders across Global Development functions to proactively identify process improvements, standardizations, and regulatory compliance that impacts the Regeneron Global Development quality system....

Regulatory Affairs Senior Associate RoleWe are seeking a highly skilled Regulatory Affairs Senior Associate to join our team at Regeneron Pharmaceuticals Inc.About the RoleThis is an exciting opportunity for a talented individual with a passion for regulatory affairs to support our CMC Regulatory submissions. As a key member of our team, you will play a...

A global pharmaceutical company, based in Uxbridge is currently looking for a Senior Regulatory Affairs Manager to join their team. You will be a confident Regulatory Lead looking to work in an innovative therapy area, developing and defining regulatory plans across multiple products. This is a great opportunity to work with a team who take provide in...

A global pharmaceutical company, based in Uxbridge is currently looking for a Senior Regulatory Affairs Manager to join their team. You will be a confident Regulatory Lead looking to work in an innovative therapy area, developing and defining regulatory plans across multiple products. This is a great opportunity to work with a team who take provide in...

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...

**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...

Parexel, a leading Clinical Research Organization (CRO), seeks an expert in Chemistry, Manufacturing, and Controls (CMC) for small molecule regulatory affairs. As a Principal Regulatory Affairs Consultant, you will lead post-approval CMC activities, providing strong project management skills and regulatory knowledge.This role offers flexibility with home or...

**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...

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...