Returning Candidate? Log back in! Director - AdPromo Job ID  4028 Location  US-NJ-Bridgewater Category  R&D - Other Pos. Type  Full Time More information about this job: Overview: Valeant Pharmaceuticals International, Inc. is a diverse and decentralized pharmaceutical company that is committed to focusing on our key stakeholders while delivering consistently high performance. Our values provide the overall direction for our company, and provide us with the tools necessary to rise to any challenge by leveraging our collective hard work and effort along with our unwavering competitive spirit. These values help us set goals based on our organization’s potential and what we hope it will become. The Director of Advertising & Promotion prescription drug products reviews, approves and monitors product advertising and promotional labeling pieces for compliance with regulatory agencies requirements. Responsibilities: ESSENTIAL DUTIES AND RESPONSIBILITIES:Represent Regulatory Affairs on the promotional review committee for marketed products to create and review promotional materials compliant with regulatory requirements while meeting Company's strategic promotional objectives.Provide guidance on proposed claims for products in development.  Develop ISI and brief summaries as appropriate.  Regularly monitor the regulatory compliance trends in industry, interpret new regulations, guidance documents and enforcement letters. Update the review committee and company regarding changes in the current regulatory environment at FDA's Office of Prescription Drug Promotion (OPDP) and other regulatory considerations that may impact business.  Develop or revise procedures as needed.Develop packages for regulatory advice, resolution of FDA action letters and leads the company in discussions with OPDP.Coordinate companywide ongoing regulatory training on regulatory issues pertaining to promotion of Company products.KEY RELATIONSHIPS:Represents regulatory affairs as an active participant on cross functional prescription product promotional review teams, consisting of members from marketing, legal, medical and regulatory affairs.Interacts with Quality related to internal audits and CAPAs, as needed.  Qualifications: EXPERIENCE:Ten+ plus years of relevant pharmaceutical experience with 8+ years of relevant regulatory affairs product advertising and promotion experience. Broad knowledge of the pharmaceutical industry.  Demonstrated ability to contribute to a continuous learning and process improvement environment. Valeant is an EEO/AA employer M/F/D/V. Options: var addthis_config = {"data_track_addressbar":true};Apply for this job onlineRefer a friend to this job Valeant Pharmaceuticals is committed to leveraging the talent of a diverse workforce to create great opportunities for our business and our people. EOE/AA. Minority/Female/Disability/Vet Go back to the welcome page Application FAQsSoftware Powered by

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