Lead Reviewer, Regulatory Affairs Advertising - Monmouth Junction

We have an opening in our Monmouth Junction NJ facility for an experienced Lead Reviewer Regulatory Affairs Advertising & Promotion to join our Regulatory Affairs team.The incumbent leads regulatory review efforts supporting advertising and promotional activities across the busin ...

We have an opening in our Monmouth Junction, NJ facility for an experienced Lead Reviewer, Regulatory Affairs – Advertising & Promotion to join our Regulatory Affairs team. · ...

We have an opening in our Monmouth Junction, NJ facility for an experienced Lead Reviewer, Regulatory Affairs – Advertising & Promotion to join our Regulatory Affairs team. · Incumbent leads regulatory review efforts supporting advertising and promotional activities across the bu ...

The US Regulatory Affairs Associate Director/Director is responsible for developing and executing regulatory strategies for all advertising and promotional activities in the United States. · This role serves as the primary expert on FDA requirements for the review of promotional ...

The US Regulatory Affairs Associate Director/Director is responsible for developing and executing regulatory strategies for all advertising and promotional activities in the United States. · Bachelor's degree in scientific discipline; advanced degree preferred. · A minimum of 7 y ...

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 ...

We are driven by patients, science, and data. We make business decisions on patients' needs and we do our best every day to realize our products' benefits for our patients. · We are dedicated to being curious and diligent when innovating, · developing, · and improving products an ...

The Associate Director will develop market access and pricing strategies for Novo Nordisk's Obesity, Diabetes and MASH therapeutic franchises with a primary focus on pipeline assets (Phase 1 through 12 months prior to launch). · This role shapes market access and pricing assumpti ...

The Clinical Medical and Regulatory CMR department at Novo Nordisk is one of the most diverse collaborative groups within the organization From healthcare provider interactions and developing implementing regulatory strategies with the FDA to providing medical education collectin ...

+Job summary · The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. · +ResponsibilitiesEvidence GenerationProvide input to Product Development Plan (PDP) and Evidence Generation Plan (EG ...

Novo Nordisk's Market Access and Public Affairs team engages diverse stakeholders to forge solutions that drive patient access to innovative products. · Lead market access strategy development for pipeline assets across all development phases (Phase 1 through 12 months prior to l ...

About Novo Nordisk's Market Access and Public Affairs team engages diverse stakeholders across political and healthcare landscapes to forge solutions that drive patient access to innovative products. · ...

We are building an intentional team culture that is made up of diverse skillsets, united by the shared belief that reinvention and learning is what fuels continuous growth. · ...

We're changing lives for a living. Are you ready to make a difference? · The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization.From healthcare provider interactions and developing and impl ...

We create and deliver human-centered experiences. Our Marketing & Patient Solutions group crafts experiences as one fully integrated organization that puts empathy at the center. We leverage data and insights to inform our decision-making processes and develop an end-to-end appro ...

The Communications Department brings the value of Novo Nordisk medicines and innovations to life through strategic communications that elevate our purpose, drive our business, foster our culture and enhance our reputation with patients, customers, employees and society in the US. ...

We are building an intentional team culture that is made up of diverse skillsets, united by the shared belief that reinvention and learning is what fuels continuous growth. · ...

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 ...

We are seeking an experienced professional to provide expert regulatory affairs support focused on advertising and promotional review activities. Our team places particular emphasis on compliance with evolving FDA regulations, · Conduct comprehensive regulatory reviews of promoti ...

+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 ...