International Regulatory Affairs Advertising and Promotion Area Lead
__jobinformationwidget.freetext.LocationText__
Marlow, BKM
- Research & Development
- On-Site
- Full-time
This vacancy has now expired. Please see similar roles below.
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.
The International Regulatory Affairs Advertising and Promotion Area Lead will be responsible for ensuring promotional and non-promotional materials and activities for Allergan Aesthetics affiliates are fair, balanced, factually accurate and adhere to Codes of Practice and internal AbbVie policies. This role will be responsible for leading affiliate level review team(s) and aligning feedback between International and Area reviewers.
Responsibilities
- Lead the UK affiliate Regulatory Affairs Advertising and Promotion team, with opportunities to lead additional teams as assigned, to ensure promotional and non-promotional materials are compliant with local regulations and codes of practice while remaining commercially competitive
- Collaborate closely with OUS affiliate promotional material teams to ensure alignment between International campaigns and local execution
- Provides regulatory position, perspective, and expertise related to advertising and promotion to internal and external customers/business partners. Maintains current knowledge of local codes of practice, regulations and guidelines that impact pharmaceutical advertising and promotion.
- Collaborates and communicates effectively through all levels of management across multiple functions (Commercial, Medical, Legal, and OEC). Recognized by organizational counterparts as a key company resource on pharmaceutical advertising and promotion. Maintains current knowledge of local codes of practice, regulations and guidance.
- 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 decision-making abilities.
- 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 affiliate advertising and promotion activities.
- 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.
- Pharmacy Master’s degree or Medical degree essential.
- Registered UK Medical signatory.
- Preferred 7-10 years of pharmaceutical experience
- Strong management skills and multi-disciplinary team management. Ability to coach/mentor junior members of material review team. Proven 3-5 years in a leadership role preferred
- Experience with products at different stages of the life-cycle
- Experience working in a complex and matrix environment
- Strong communication skills, both oral and written
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 https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html
We have recently become aware of various recruitment phishing scams targeting job seekers. Please be advised:
- AbbVie will never request sensitive personal information (such as bank account details, social security numbers, or payment of any kind) during the recruitment process.
- If you suspect you have received a fraudulent offer or communication claiming to be from AbbVie, please do not respond, open any attachments, or click on any hyperlinks.
If you have any questions or concerns regarding the authenticity of a communication alleged to have been made by or on behalf of AbbVie, please contact us immediately.
Protect yourself by verifying job offers and communications. Your safety is important to us.
Pay Range: $
-
Where We Work
Role is exclusively performed at a site or office and onsite presence is required. Employees who are site/office-based and can occasionally perform their role virtually work both in the office and remotely*, following the policies and regulations in place at their location. US Employees must be in the office on Tuesday, Wednesday, and Thursday with flexibility to work remotely on Mondays and Fridays. Three days in the office is the minimum; some individuals or teams may require more in-office days due to meetings, business/project needs or their role.