Director of Global TA Regulatory Strategy

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...

Key ResponsibilitiesAs a Regulatory Affairs Senior Manager, you will be responsible for operating as a Regulatory Lead, providing centralised regulatory strategy and guidance across the region.Your key responsibilities will include:Developing, contributing, and ensuring the accurate preparation of high-quality regulatory documents needed to support clinical...

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: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...

Unlock a Challenging Career Opportunity in Life SciencesLifelancer is seeking an exceptional Senior Director to join our team in the Field Medical Excellence department. As a key member of our organization, you will play a pivotal role in ensuring that healthcare professionals are educated on the appropriate use of our medicines and have the information they...

**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...

Unlock Your Potential as a Regulatory Affairs DirectorBristol-Myers Squibb, a leader in precision medicine and digital health, seeks an experienced Regulatory Affairs Director to join our team. This is a challenging role that requires expertise in global regulatory strategy, leadership skills, and a passion for transforming the lives of patients.About the...

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...

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...

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,...

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...

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...

Lifelancer is a talent-hiring platform that connects professionals with opportunities in the life sciences, pharmaceuticals, and IT sectors. We are committed to providing our clients with exceptional talent and fostering a collaborative work environment.We are seeking a Senior Director, International Field Medical Excellence to join our team. This role will...

Description The GRS-CMC organization provides regulatory expertise related to CMC activities through all stages of a products lifecycle. Members of the organization develop global regulatory CMC strategies and partners with key stakeholders to execute the strategies in alignment with business priorities. The team also perform regulatory assessments...

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...

About the RoleAs a Regulatory Affairs Manager, you will play a key role in planning and managing regulatory submissions (e.g., clinical trial and marketing applications) for products within our portfolio in compliance with global filing plans and local regulatory requirements.You will also be responsible for acting as a contact with relevant regulatory...