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AbbVie (NYSE:ABBV) is a global, research-driven biopharmaceutical company committed to developing innovative advanced therapies for some of the world’s most complex and critical conditions. The company’s mission is to use its expertise, dedicated people and unique approach to innovation to markedly improve treatments across four primary therapeutic areas: immunology, oncology, virology and neuroscience. In more than 75 countries, AbbVie employees are working every day to advance health solutions for people around the world.  For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook or LinkedIn.​

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Associate Director, Regulatory Affairs, Global Regulatory Strategy, US & Canada

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Research & Development
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1805943 Requisition #

The Associate Director, Regulatory Affairs, Global Regulatory Strategy, US and Canada has primary responsibility for the development and implementation of US and Canada regulatory strategic and tactical planning (RSTP) for assigned on market products or those products in development. These responsibilities are carried out in collaboration with key internal stakeholders from within Regulatory Affairs including those on the Global Regulatory Project Team (GRPT) (i.e., CMC Regulatory, Labeling, Advertising and Promotion), ABBV Canada Affiliate Regulatory Team, and cross functional colleagues (e.g. Clinical Development, Commercial, Marketing, Product Safety), on the Integrated Brand Team. This individual demonstrates the ability to combine knowledge of scientific, regulatory & business issues to enable development and commercialization of products that are developed, manufactured or distributed to meet relevant US and Canada regulatory requirements.

 

Key Responsibilities Include:

  • This individual has responsibility for products/multiple driver indications for a product within a Therapeutic Area and supports the Global Regulatory Lead (GRL, Director), in the development & execution of the regulatory strategy
  • Represents US/C Global Regulatory Strategy on the Integrated Brand Team
  • Serves as US and Canada (US/C) Regulatory Lead on the Global Regulatory Product Team (GRPT)
  • Area of responsibility has significant regulatory impact and possibly significant impact to ABBV overall
  • Manages interface with Health Authority (FDA) for key projects/issues, including direct collaboration with review division personnel
  • May also serves as primary liaison and interfaces with FDA for meetings, teleconferences and coordinates preparation of FDA meeting briefing packages and responses
  • Demonstrates effective communication skills in written and oral channels both within Regulatory and across the organization
  • Advise internal customers who may contribute to regulated communication on Regulatory/FDA issues including Public Affairs, Clinical Development, Legal, and others such as Commercial
  • Demonstrates excellent negotiation skills, problem solving skills and builds consensus
  • Able to deliver challenging messages effectively without compromising important business relationships
  • Establishes solid relationships with management and key stakeholders fostering mutually beneficial interactions
  • Operates independently, with recognition of when to consult management
  • Makes decisions and plans for operations (work flow, assignments, staff development) within area of responsibility with minimal direction
  • Assists in the development, training, and mentoring of staff members
  • Encourages innovation and holds employees accountable for delivering on their goals; recognizes, mentors, rewards and recommends promotion for staff members based on their performance, results, and development
  • Coordinates, prepares and/or supervises the preparation and review of regulatory submissions consistent within US and Canada regulatory requirements and guidelines and assures complete and timely response to Health Authorities during application review
  • Ensures application of established policies and best practice regulatory standards for all US/Canada product registrations
  • Demonstrates solid understanding of current US and Canada regulations and guidance, political and legal climate and industry practices to assist in meeting organizational goals
  • Broadly applies regulatory/technical knowledge of government regulations and skills across therapeutic areas and is generally recognized as a resource & leads the department as a subject matter expert (SME) for Regulatory
  • Uses problem solving skills to separate and combine tasks into efficient workflow and effectively/creatively solve complex and difficult problems
  • Presents pertinent regulatory information to appropriate cross-functional areas.
  • Provides input into the budget, identifies and communicates budgetary needs, and identifies current and future expenditures and business needs
  • Provide budgetary input into the use of contractors and consultants.
  • Operates in compliance with regulations, company policies, procedures, and guidance in alignment with regulatory product strategy and the Quality Dossier Program (QDP).
  • Bachelor’s Degree (pharmacy, biology, pharmacology) or related life sciences
  • Relevant advanced degree is preferred
  • Certification a plus
  • 8 years Regulatory, R&D or Industry-related experience
  • 5 years in pharmaceutical regulatory affairs
  • Extensive experience interfacing with government Agencies and Health Authority personnel.
  • Experience working in a complex and matrix environment
  • Demonstrated success in negotiation skills, strategic thinking, and credibility within the organization
  • Strong communication skills, both oral and written
  • Proven skill at implementing successful US and Canada regulatory strategies; global regulatory experience is a plus

 

Equal Opportunity Employer Minorities/Women/Veterans/Disabled

 

Travel:

10-15% Travel

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