Global Head of Regulatory Affairs

About the RoleWe are seeking a highly skilled and experienced Regulatory Affairs Director to join our team at GlaxoSmithKline. As a key member of our Global Regulatory Affairs team, you will play a critical role in shaping our regulatory strategy and ensuring compliance with regulatory requirements.Key ResponsibilitiesDevelop and implement regulatory...

The Director of Regulatory Affairs at The Steely Group plays a pivotal role as a liaison with Health Authorities and leads regulatory projects across various development phases. This position demands a strategic regulatory expert who will guide drug development initiatives, leveraging extensive expertise to inform project teams on compliance requirements and...

The Director of Regulatory Affairs at The Steely Group plays a pivotal role as a liaison with Health Authorities and as a leader in regulatory projects across various development phases. This position is essential for guiding drug development initiatives and leveraging extensive regulatory knowledge to support project teams in navigating complex...

**This position requires 3 days onsite in Cambridge**The role acts as a liaison with Health Authorities and serves as the Regulatory Project Leader for various initiatives at different stages of development. Responsibilities include:Strategic LeadershipProvides expert regulatory guidance for assigned drug development projects, leveraging extensive knowledge...

The Director of Regulatory Affairs at The Steely Group plays a pivotal role as a liaison with Health Authorities and leads regulatory projects across various development phases. This position demands a strategic regulatory leader who can effectively guide drug development initiatives by leveraging extensive expertise in regulatory frameworks.Key...

Job SummarySarepta Therapeutics is seeking a highly experienced Regulatory Strategy Director to lead our regulatory affairs efforts. As a key member of our team, you will be responsible for developing and implementing regulatory strategies that ensure compliance with global regulations and facilitate the approval of our therapeutic programs.Key...

Job SummaryWe are seeking a highly experienced and skilled Director of Regulatory Affairs and Quality to lead our Regulatory Affairs and Quality teams in the development and execution of compliant regulatory strategies and quality team/QMS responsibilities.Key ResponsibilitiesRegulatory Affairs Strategy and ExecutionDevelop and execute end-to-end regulatory...

The Director of Regulatory Affairs at The Steely Group plays a pivotal role as a liaison with Health Authorities and as a leader for various regulatory projects at different stages of development. This position requires a strategic mindset to guide drug development initiatives and ensure adherence to regulatory standards.Key Responsibilities:Oversees the...

Job TitleRegulatory Affairs Senior ManagerJob SummaryPhilips is seeking a highly experienced Regulatory Affairs Senior Manager to lead regulatory projects for Philips Clinical Informatics organization. The successful candidate will play a critical role in ensuring and maintaining global accurate regulatory strategy and market access for Philips Disease...

Job Title: Regulatory Affairs Senior SpecialistJob Description:In light of the pressing challenges our world faces today, the mission of Philips has never been more significant. If you share our commitment to enhancing lives, your contributions will be pivotal in shaping a more equitable future for everyone.In this position, you will have the opportunity...

The Director of Regulatory Affairs at The Steely Group plays a pivotal role as a liaison with Health Authorities and leads regulatory projects across various development phases. This position demands a strategic regulatory leader who will guide drug development initiatives by leveraging extensive expertise to inform project teams on regulatory standards,...

About the RoleWe are seeking a highly experienced Regulatory Affairs Director to lead our medical devices, molecular testing, and biomarkers regulatory strategy and oversight. As a key member of our team, you will be responsible for ensuring that our products meet the highest regulatory standards and are compliant with global regulations.Key...

The RoleModerna is seeking a Director, Global Medical Affairs to spearhead Medical Affairs activities for our Oncology Individualized Neoantigen Therapy (INT) program.Reporting into the Vice President, Global Medical Affairs Oncology, this role will be the primary point person for the development of INT Medical Affairs plans and strategic activities,...

The Role:Moderna, Inc. is seeking a Director of Regulatory Strategy to develop and lead global strategy for mRESVIA, Modernas late stage / marketed RSV messenger RNA (mRNA) vaccine (Adult indication) to be based in one of Modernas East Coast hubs. The Global Regulatory Lead (GRL) role is intended for a forward looking, creative regulatory strategist able to...

The Role:Moderna, Inc. is seeking a Director of Regulatory Strategy to support INT within the Oncology programs. This is a newly created role intended for a forward looking, creative regulatory strategist able to anticipate and address the challenges involved in gaining market approval for messenger RNA oncology products as unprecedented new drug modality in...

Position OverviewAt Takeda, we are committed to pioneering advancements in research and development that lead to transformative therapies for patients. Our focus on four key therapeutic areas, along with targeted investments, allows us to redefine the possibilities in delivering life-altering treatments globally.As the Senior Director of Regulatory Affairs...

Position OverviewKytopen is at the forefront of enhancing cell engineering for advanced cell therapies, aiming to broaden access to innovative living medicines. Our unique continuous Flowfect non-viral transfection platform is designed to deliver rapid, scalable, and gentle processes that produce billions of high-quality engineered cells in mere minutes...

How you will Achieve More with Intellia:We are hiring a Head of Development for Ex Vivo Programs to oversee all functions for the ex vivo programs, including clinical, regulatory, and biometrics.You will act as a Program Team Lead for an innovative new Ex Vivo Cell Therapy Program.You will be responsible for the development and execution of short and...

The Role:Moderna Therapeutics is seeking an Associate Director of Regulatory Strategy to support programs within the oncology franchise to be based in one of Modernas US offices. This is a role intended for a forward looking, creative and agile regulatory strategist able to anticipate and address the challenges involved in developing and registering oncology...

Job Summary:Proclinical Staffing is seeking a highly experienced Director, Global Regulatory Labeling to join our team. As a key member of our organization, you will be responsible for developing and executing regulatory labeling strategies for our global biotech clients.Key Responsibilities:Regulatory Labeling Strategy: Develop and maintain current...