Lead Reviewer, Regulatory Affairs Advertising - Monmouth Junction

We have an opening in our Monmouth Junction facility for an experienced Lead Reviewer to join our Regulatory Affairs team.The incumbent partners closely with cross-functional teams to ensure compliance with regulatory requirements while driving strategic promotional initiatives. ...

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 Associate Director, Regulatory Affairs, Advertising and Promotion Compliance will independently review, · approve, · and monitor product advertising · & promotional labeling material for an assigned product to ensure compliance with US regulatory requirements.In addition, · t ...

The Associate Director Regulatory Affairs will independently review approve and monitor product advertising promotional labeling material for assigned products to ensure compliance with US regulatory requirements. The Associate Director is responsible for providing strategic tact ...

· Kyowa Kirin is a fast-growing global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in four disease areas: bone and mineral; intractable hematologic; hematology oncology; and rare disease.  A Japan-based c ...

The Associate Director will independently review, approve and monitor product advertising for assigned products to ensure compliance with US regulatory requirements. · ...

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 ...

· Tris Pharma, Inc. ) is a leading privately-owned US biopharmaceutical company focused on development and commercialization of innovative medicines in ADHD, spectrum disorders, anxiety, pain and addiction addressing unmet patient needs. We have >150 US and International patents ...

Tris Pharma, Inc. ) is a leading privately-owned US biopharmaceutical company focused on development and commercialization of innovative medicines in ADHD, spectrum disorders, anxiety, pain and addiction addressing unmet patient needs. We have >150 US and International patents an ...

We have an opening at our Monmouth Junction, NJ facility for an experienced Director or Associate Director, Marketing.The Director/Associate Director Marketing leads development and implementation of US Health Care Provider (HCP) marketing strategy, · launch marketing plan and om ...

:Tris Pharma, Inc. ) is a leading privately-owned US biopharmaceutical company focused on development and commercialization of innovative medicines in ADHD, spectrum disorders, anxiety, pain and addiction addressing unmet patient needs. We have >150 US and International patents a ...

Title: Senior Director, Regulatory Advertising & Promotion, Medical Affairs, Princeton, NJ - Hybrid · Date: Feb 23, 2026 · Location: Sun - Princeton - Corporate Office · Company: Sun Pharmaceutical Industries, Inc (USA) · Job Summary: · Sun is seeking a Senior Director, Regulator ...

We have an opening at our Monmouth Junction, · NJ facility for an experienced Director or Associate Director, · Marketing.The Director/Associate Director Marketing leads development · and implementation of US Health Care Provider (HCP) marketing strategy, ...

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 ...

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. · ...

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 ...

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 ...