Regulatory Affairs Director
Regulatory Affairs Director
Posted on :
02-05-2025
Employer Active
1 Vacancy
Job Alert
You will be updated with latest job alerts via emailValid email field required
Send jobs
Share
Send me jobs like this
Job Alert
You will be updated with latest job alerts via emailValid email field required
Send jobs
Job Description
Responsibilities
- Provides International regulatory position perspective and expertise related to advertising and promotion to internal and external customers/business partners. Maintains current knowledge of international codes of practice regulations and guidance that impacts pharmaceutical advertising and promotion.
- Collaborates and communicates effectively through all levels of management across multiple functions (Commercial Medical Legal and Compliance). Recognized by organizational counterparts as a key company resource on pharmaceutical advertising and promotion. Applies novel and creative methods to problem solving. Constantly searches for out of the box solutions while maintaining quality and adherence to regulations. Balances business needs and risk assessments with creative decisionmaking abilities.
- Manages a team of material reviewers and final signatories responsible for ensuring compliant International marketed and development compounds advertising and promotion strategies. Has accountability for the sound representation of International Regulatory Advertising and Promotion position within and external to Allergan Aesthetics. Defines boundaries of accepted risk tolerance within assigned programs.
- Maintains current knowledge of international codes of practice regulations and guidance. Demonstrates compliance with international codes of practice relevant regulations and manages financial business goals. Provide input into brand strategy and key asset and therapy area initiatives as required.
- Reviews and evaluates the global industry environment (e.g. regulatory legal and political climate) and competitive landscape (e.g. product strategies commercial messages positioning etc.. Provides functional input on key initiatives impacting other areas. Leads the implementation of risk management strategies and risk management plans for International advertising and promotion activities.
- Lead operations initiatives and strategies for the International Regulatory Affairs Advertising and Promotion team.
- Share best practice and contribute to the development of marketing campaigns from concept creation and through in collaboration with crossfunctional partners.
- Provide guidance on International codes to affiliate markets as and when required and when required and confidently present competitive landscape cases to encourage team learning
- Supports departmental and business strategies quality initiatives compliance with policies and procedures and the implementation of improvement plans. Contributes to the evaluation of departmental needs and implements solutions to enhance and facilitate operations.
- Creates an environment to attract retain empower and mentor future leaders across Regulatory Advertising and Promotion.
Qualifications :
- Preferred 710 years of pharmaceutical experience with a minimum of 5 years direct advertising and promotion regulatory experience
- Minimum Bachelors Degree (or equivalent) in science (biology chemistry microbiology immunology medical technology pharmacy pharmacology) is required. Masters or Ph.D. preferred. Registered medical practitioner or pharmacist in the UK preferred.
- Registered signatory or successful completion of Abbvie qualifications to become a registered signatory preferred.
- The candidate must have a solid understanding of advertising and promotion regulations and UK and International Codes of Practices having had direct responsibility in this area.
- Strong management skills and multidisciplinary team management. Proven 35 years in a leadership role preferred
- Experience with products at different stages of the lifecycle
- Experience working in a complex and matrix environment
- Strong communication skills both oral and written
Additional Information :
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
No
Employment Type :
Fulltime
Employment Type
Full-time
Key Skills
Report This Job
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.
