US - Assistant Global Labeling Lead - Princeton, NJ

The Assistant Global Labeling Lead (AGLL) will support Freyr's Client by assisting the Global Labeling Lead (GLL) in authoring, reviewing, and maintaining key labeling documents such as Core Company Data Sheets (CCDS), US Prescribing Information (USPI), and local labeling across ...

The Global Labeling Lead (GLL) has overall accountability for the initial creation and relevant updates to labeling documents for their assigned products. · Utilize regulatory, labeling and project management expertise to oversee and support the development, review · and delivery ...

Drive Labeling Strategy in-line with overall global regulatory strategy by providing labeling expertise. Facilitate strategic development of labeling and components by leading cross-functional teams. · ...

The Director of Global Labeling Strategy will provide labeling expertise for Company Core Data Sheet (CCDS), USPI and local labeling from early-stage development through to product maintenance. · ...

Taiho Oncology is on a mission to improve the lives of patients with cancer, their families, and caregivers. · Develop, update, and maintain auto-labeling data sheets for the safety database. · Ensure labeling documents such as USPI are current for assessment of ICSRs. · ...

The Established Brands Associate Director Medical Affairs is responsible for leading and executing medical strategy and activities for brands within the expanding Established Brands portfolio. · ...

The Established Brands Associate Director Medical Affairs is responsible for leading and executing medical strategy and activities for brands within the expanding Established Brands portfolio. ...

Provides strategic direction for clinical supply chain planning activities for assigned programs in the R&D Portfolio. · ...

We offer an opportunity for you to learn and grow while making significant contributions to the company's success. · SystImmune is seeking a high quality, ambitious and experienced Clinical Supplies Manager to support SystImmune's clinical trials.The Clinical Supplies Manager is ...

SystImmune is seeking a high quality Clinical Supplies Manager to support SystImmune's clinical trials. · ...

Joining us is a chance to do important work that creates change and shapes the future of healthcare. · Thinking differently is what we do best. To us, change equals opportunity. · Every day our colleagues are challenging what's possible and making headway to innovate new treatmen ...

The Associate Director is responsible for leading medical strategy and activities for established brands within Bristol Myers Squibb's expanding portfolio. · Partner with cross-functional partners to ensure appropriate medical support. · ...

Transforming patients' lives through science working at Bristol Myers Squibb is anything but usual here uniquely interesting work happens every day in every department you'll get the chance to grow and thrive through opportunities uncommon in scale and scope alongside high-achiev ...

The Princeton University Art Museum seeks a Research Assistant for a position beginning in February 2026 and lasting approximately 17 weeks. · ...

+Job summary · Lensa does not hire directly for these jobs, but promotes jobs on LinkedIn on behalf of its direct clients. · +Serve as the medical/scientific reviewer of promotional assets for assigned product(s), and collaborate with Commercial, Legal, and Regulatory for develop ...

The Director Drug Safety Physician is responsible for leading Global Safety Teams in developing safety strategies ensuring patient safety and regulatory compliance for products in development and/or marketed. · ...

The Director Drug Safety Physician is responsible for leading the Global Safety Team(s) to develop safety strategies ensure patient safety regulatory compliance products in development marketed. · ...

We offer an opportunity for you to learn and grow while making significant contributions to the company's success.The Regulatory Affairs (Clinical/Nonclinical) role will drive regulatory strategy and execution within SI Project development teams and the RA Department in all aspec ...

This is an opportunity to work at Bristol Myers Squibb as an Associate Director in US Commercial Regulatory Affairs. The role involves applying complex scientific and expert regulatory advice to ensure promotional campaigns meet the company's objectives. · Provides regulatory adv ...

· SystImmune is seeking an experienced Director/Sr. Director/Executive Director for its Clinical Regulatory Affairs team to drive regulatory strategy and execution within SI Project development teams. · Integrate scientific, medical and regulatory perspectives to drive developme ...