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 Twitter, Facebook, Instagram, YouTube and LinkedIn. 

The Senior Manager Regulatory Affairs US Advertising and Promotion combines knowledge of scientific, regulatory, and business issues to enable products that are developed, manufactured or distributed to meet regulatory requirements. Additionally, the individual develops and supervises regulatory professionals as needed. Has department/group/site level influence and is generally recognized as an expert and resource and leads the department as a subject matter expert (SME) for Regulatory Affairs in cross-functional workstreams.  Shares knowledge and expertise with others in support of team activities. Analyzes broad scope implications of changing regulations and policies.

Responsibilities:

• Reviews promotional and non-promotional communications for on-market products to ensure compliance with applicable laws and regulations, as well as internal policies and procedures. Functions independently in this role while bringing relevant topics to management as appropriate.
• Provides regulatory guidance for data and information consistent with product labeling.
• Participates in pipeline commercialization activities; reviews and contributes to target product claims, target product labeling.
• Acts as a key contributor on cross-functional teams and workstreams for pipeline and on-market products.
• Develops and guides implementation strategies for promotional activities.
• Broadly applies regulatory/technical knowledge of government regulations and skills across therapeutic areas.
• Proactively captures and disseminates activities of government, industry, and trade associations that impact pharmaceutical regulatory policies relative to AbbVie’s interests. Maintains awareness of pending changes to communicate impact and relevance within US Advertising and Promotion department.
• Represents department and participates in trade associations as needed.
• Summarizes findings, under supervision, in concise reports for distribution within AbbVie
• If assigned staff, oversees their operations, productivity, and development.
• Ensures departmental training and compliance with established regulations, FDA guidance, promotional guidelines, and SOPs related to advertising and promotion regulations. If applicable, manages direct reports and assist in the development, training and mentoring of staff members
• Effectively presents pertinent information to appropriate cross-functional groups.
• Effectively delivers difficult messages to commercial organization while maintaining relationships.
• Establishes good working relationships with management and key stakeholders (Marketing, Medical, Clinical, Legal, Sales Training, Market Access, Public Affairs, etc.), fostering mutually beneficial interactions and exchange.

This role can be based remotely within the US. 

• Bachelor’s degree in science (biology, chemistry, microbiology immunology, medical technology pharmacy, pharmacology, nursing, pharmacy) Relevant Master’s degree (Pharmacy, advanced scientific or law) preferred
• 7 years pharmaceutical experience in Regulatory Affairs or related area preferred.
• Experience working in a complex and matrix environment and exhibits strong negotiation skills.
• Strong communication skills, both oral and written
• Experience in management capacity preferred
• Experience in US Regulatory Affairs Advertising and Promotion preferred.

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​

​

• The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.​

• 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 short-term incentive programs. ​

• This job is eligible to participate in our long-term incentive programs​

​

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. 

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion.  It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.

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