Director, Global Labeling Strategy - Princeton, NJ

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 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 ...

About Freyr.Freyr Inc. is a global leader in regulatory solutions and services within the life sciences industry. · The Assistant Global Labeling Lead (AGLL) will support Freyr's Client by assisting the Global Labeling Lead (GLL) in authoring, reviewing, and maintaining key label ...

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. · ...

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. ...

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 ...

We are seeking a Regulatory Affairs Professional who will serve as an internal expert on U.S. FDA regulations governing the promotion of prescription drug and biologic products.The ideal candidate will have experience in drug, biologic and/or combination products in Regulatory Af ...

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

+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 ...

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 Head of Established Brands will be responsible for leading the strategy and positioning of the company's established portfolio spanning dermatology ophthalmology and oncology This role offers the opportunity to strengthen and grow a ~$45M portfolio while also preparing for ne ...

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 ...

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. · ...

The Director of Global HEOR - Oncology is responsible for planning and leading the health economics and outcomes research (HEOR) evidence generation strategy, · Independently lead the strategy, design and execution of robust evidence generation of HEOR studies ...

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 ...

· 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 ...

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 Clinical Account Executive will report into the Commercial- Rare Disease Team at ANI. The position requires performance driven individuals with strategic problem- solving skills and high business acumen that can work collaboratively with multiple stakeholders. · ...