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International Regulatory Affairs Advertising and Promotion Area Lead

International Regulatory Affairs Advertising and Promotion Area Lead

International Regulatory Affairs Advertising and Promotion Area Lead

International Regulatory Affairs Advertising and Promotion Area Lead

AbbVie

Pharmazeutische Produkte, Arzneimittel

Marlow

  • Art der Beschäftigung: Vollzeit
  • 63.000 € – 89.000 € (von XING geschätzt)
  • Vor Ort
  • Zu den Ersten gehören

International Regulatory Affairs Advertising and Promotion Area Lead

Über diesen Job

What AbbVie Has to Offer:

Our work can—and does—have a tangible, lasting impact on millions of people. But it’s not just the results that matter. How we achieve them matters, too. Leading with purpose, we work to build a more sustainable future for generations to come. We do that by putting our expertise, resources and talent to work to make a real difference for patients, communities and our world.

Job Details


Company Description

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 .

Job Description

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.

Qualifications

  • 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

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 https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

Gehalts-Prognose

Unternehmens-Details

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AbbVie

Pharmazeutische Produkte, Arzneimittel

10.001 oder mehr Mitarbeitende

Wiesbaden, Deutschland

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