Global Regulatory Lead, Oncology

Responsibilities: Develop global regulatory strategy for Oncology products in development and through life cycle management considering all relevant guidance, commercial needs, and company objectives. Develop global or US regulatory strategy for Oncology products in development and through life cycle management, considering all relevant guidance,...

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...

Sunrise System Inc. is currently looking for Global Regulatory Strategist in Lawrenceville, Summit, New Brunswick, Warren, NJ OR Tampa, FL, Hybrid 50% with one of our top pharma client.Job Title: Regulatory & Medical Affairs - Global or US Regulatory StrategistLocation: Lawrenceville, Summit, New Brunswick, Warren, NJ OR Tampa, FL, Hybrid 50%Duration: 12...

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...

Sunrise System Inc. is currently looking for Global Regulatory Strategist in Lawrenceville, Summit, New Brunswick, Warren, NJ OR Tampa, FL, Hybrid 50% with one of our top pharma client.Job Title: Regulatory & Medical Affairs - Global or US Regulatory StrategistLocation: Lawrenceville, Summit, New Brunswick, Warren, NJ OR Tampa, FL, Hybrid 50%Duration: 12...

Join a Legacy of Innovation 110 Years and CountingDaiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class scienceand technology. With more than 100 years of scientific expertise and a presence...

Join a Legacy of Innovation 110 Years and CountingDaiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class scienceand technology. With more than 100 years of scientific expertise and a presence...

Purpose Ensure the development of appropriate Precision Medicine and Digital Health regulatory strategy(s) and their execution for assigned precision medicine and digital health asset(s) supporting across the GSK therapeutic portfolio. This goal must be achieved both as a component of an overall global regulatory approach and ensure compliance with both...

Purpose Ensure the development of appropriate Precision Medicine and Digital Health regulatory strategy(s) and their execution for assigned precision medicine and digital health asset(s) supporting across the GSK therapeutic portfolio. This goal must be achieved both as a component of an overall global regulatory approach and ensure compliance with both...

Regulatory Affairs Specialist Project Lead I (Scientific)REMOTE06 MonthsRequires candidates that have worked on medicinal products (small molecule or biologic) marketing applications-- like NDA, BLA, MAA.Description:This role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies and be...

Job Purpose: Leads CMC regulatory activities in the global lifecycle management of GSK biopharmaceutical products. Management oversight for a team ensuring compliance with GSK policies and procedures, staff development and training to deliver roles. Key Responsibilities: Represents Global CMC Regulatory, on Regulatory Networks and Matrix Teams...

Are you looking for a highly visible role where you can ensure the development and execution of appropriate strategies across all stages of the product life cycle consistent with the Vaccines Development Strategy/Integrated Asset Plan (IAP)? If so, this role could be an exciting opportunity to explore. Accountable to the asset GRL and/or the Global...

About the Department Our East Coast Global Development Hub brings together the best minds in life science innovation with facilities in Lexington, MA and Plainsboro, NJ. We support programs from early research through late-stage clinical development. We are building for the future, creating a distinct R&D community based on collaboration,...

About the Department Our East Coast Global Development Hub brings together the best minds in life science innovation with facilities in Lexington, MA and Plainsboro, NJ. We support programs from early research through late-stage clinical development. We are building for the future, creating a distinct R&D community based on collaboration,...

Lead Health is seeking a travel nurse RN Oncology for a travel nursing job in Neptune, New Jersey. Job Description & Requirements Specialty: Oncology Discipline: RN Start Date: 06/17/2024 Duration: 13 weeks 36 hours per week Shift: 12 hours, nights Employment Type: Travel We need a Oncology Travel RN to make a positive impact on patient care! There...

Job Title: Senior Manager, Global Labeling Strategy Job ID: (phone number removed) Location: Lawrenceville, NJ, 08648   Senior Manager, Global Labeling Strategy has overall accountability for relevant updates to labeling documents (Company Core Data Sheet (CCDS), United States Package Inserts (USPI) and EU Summary of Product Characteristics (SmPC) for...

Job Title: Senior Manager, Global Labeling StrategyJob ID: (phone number removed)Location: Lawrenceville, NJ, 08648Senior Manager, Global Labeling Strategy has overall accountability for relevant updates to labeling documents (Company Core Data Sheet (CCDS), United States Package Inserts (USPI) and EU Summary of Product Characteristics (SmPC) for products...

Are you looking for a highly visible regulatory leadership role where you can build advocacy and accelerate regulatory compliance on a global scale? If so, this Regulatory Affairs Management Director role could be an exciting opportunity to explore. As Director, Regulatory Affairs-Specialty, you will ensure the development of appropriate regulatory...

**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...

Working with UsChallenging. 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 the...