Manager Regulatory Affairs, US Advertising and Promotion

Responsibilities

• Effectively presents pertinent information to appropriate cross-functional groups
• Responsible for high impact and visible departmental project(s). Provides leadership in problem solving with teams
• Functions as the expert within the job function and the product/disease state. Rapidly understands, evaluates and identifies issues/problems
• Develops and executes departmental and therapeutic area strategies
• Mentors staff, contractors interns and/or rotational students
• Employs rigorous logic and methods to independently and effectively/creatively solve difficult problems. Probes multiple sources for answers. Identifies hidden problems and issues beyond the obvious
• Develops solutions for more complex issues with little guidance from management
• Proactively addresses and resolves issues having potential impact on working relationships and productivity
• Uses problem solving skills to separate and combine tasks into efficient workflow, makes good decisions based upon a mixture of analysis, experience and judgment.
• This role will work a hybrid work schedule (3 days in office) from the Mettawa, IL; Irvine,CA or Florham Park, NJ AbbVie headquarters.
• Significant Work Activities: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hr day) is required
• Minimum: Bachelor's degree in science (biology, chemistry, microbiology immunology, medical technology, pharmacy, pharmacology, nursing, pharmacy) + 6 years of relevant industry experience (e.g. regulatory affairs including fellowships, Health Authority, ad promo, etc.)
• Relevant Master's degree (Pharmacy, advanced scientific or law degree ) PharmD degree preferred plus 3 years of relevant industry experience
• Experience working in a complex and matrix environment
• Exhibits strong negotiation skills plus strong communication skills, both oral and written
• Experience in US Regulatory Affairs Advertising and Promotion
• Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
• This job is eligible to participate in our long-term incentive programs.
• 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

Benefits

Additional Information

The Manager Regulatory Affairs US Advertising & Promotion, combines knowledge of scientific, regulatory and business issues to enable products that are developed, manufactured or distributed to meet required legislation. The Manager is responsible for 1-2 of the following: therapeutic area, products or multiple driver indications for a product; develops and supervises regulatory professionals as needed. The Manager has department/group/site level influence and is generally recognized as an expert and resource within the department; supports the Director in efforts to influence the regulatory environment; shares knowledge and expertise with others in support of team activities; and analyzes broad scope implications of changing regulations and policies.

Your Match

How well this role fits your profile.

Company Intel

What employees say

Worked at Abbvie? Share your experience