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Director, Regulatory Advertising, Promotional & Scientific Messaging
Lundbeck. Serve as US Regulatory Affairs advertising and promotion strategic partner for assigned brands across launch and lifecycle management .
Posted 10/26/2026full-timeBoston • Massachusetts • United StatesLead💰 $200,000 - $225,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates extensive expertise in US Pharmaceutical Advertising and Promotion Regulatory Strategy, with a strong ability to lead complex promotional reviews and navigate FDA interactions. Proven track record in developing compliant solutions and guiding communication strategies across multiple audiences and channels.
Highest-signal resume keywords
US Pharmaceutical Advertising And Promotion Regulatory StrategyFDA Promotional Regulations And GuidancePromotional Review And Strategy LeadershipScientific Data EvaluationCross-Functional Collaboration
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Regulatory ReviewClaims AssessmentPromotional ComplianceRegulatory Risk AssessmentFDA Interaction ManagementAdvertising And Promotion StrategyScientific MessagingLifecycle ManagementNegotiation SkillsCommunication Strategy Development
Soft Skills
Interpersonal SkillsWritten CommunicationOral CommunicationIndependent JudgmentCollaboration
Certifications & Qualifications
Accredited Bachelor’s Degree
Industry Keywords
Pharmaceutical IndustryBiotechnologyMedical Device IndustryRegulatory AffairsAdvertising And PromotionHCP CommunicationDTC CommunicationMarket AccessCorporate CommunicationsMatrixed Environment
About the role
Key responsibilities & impact- Serve as US Regulatory Affairs advertising and promotion strategic partner for assigned brands across launch and lifecycle management
- Lead regulatory review and assessment of claims, advertising, and promotional materials for accuracy, approved-label consistency, and FDA/internal compliance
- Represent Regulatory in Medical, Legal and Regulatory (MLR) review and other cross-functional forums
- Assess complex issues, articulate regulatory risk, negotiate positions, and develop compliant, commercially enabling solutions
- Guide scientific and promotional concepts and communication strategies for HCP, DTC, payer, pipeline, digital, social media, patient, advocacy, and other external communications
- Lead promotional compliance activities for launch planning and commercialization
- Lead interactions with FDA/OPDP regarding advertising and promotion, including advisory comments
- Partner with Commercial, Medical, Legal, Market Access, Corporate Communications, Regulatory Affairs, brand teams, and other stakeholders
- Build trusted relationships and communicate regulatory positions and recommendations across organizational levels
- Monitor US advertising and promotion regulatory developments and translate them into actionable recommendations
- Provide regulatory leadership, coaching, and subject-matter expertise across matrixed teams
Requirements
What you’ll need- Accredited Bachelor’s degree
- 10+ years of R&D, regulatory or related experience within the pharmaceutical, biotechnology, and/or medical device industry
- 5+ years in the advertisement, promotional and scientific messaging area
- Extensive, hands-on experience in US pharmaceutical advertising and promotion regulatory strategy and review of external communications for multiple audiences and channels
- Demonstrated ability to lead complex promotional review and strategy, including interpretation and application of FDA promotional regulations and guidance
- Experience assessing product claims and supporting scientific evidence across HCP and DTC
- Strong knowledge of FDA requirements governing prescription drug and/or biologic advertising and promotion
- Experience navigating FDA interactions, including OPDP communications
- Ability to assess complex or novel regulatory issues, establish and communicate regulatory positions, articulate risk-based decisions, and develop pragmatic compliant solutions
- Strong understanding of scientific data and ability to critically evaluate scientific evidence supporting promotional claims and communications
- Strategic leadership and ability to influence at multiple levels in a highly matrixed environment
- Experience supporting product launches and lifecycle management from an advertising and promotion regulatory perspective
- Excellent negotiation, interpersonal, written, and oral communication skills
- Ability to manage multiple priorities, exercise independent judgment, and deliver high-quality work within established timelines
- Ability to work independently and collaborate effectively within multidisciplinary, matrixed, and potentially global teams
- Willingness and ability to travel domestically and internationally up to approximately 20%
- Strong preference to be based in Boston, MA area
- If based remotely, ability to travel additionally to Boston, MA as required
Benefits
Comp & perks- Eligibility for a 25% bonus target based on company and individual performance
- Eligibility to participate in the company’s long-term incentive plan
- Flexible paid time off (PTO)
- Medical, Dental and Vision health benefits
- Company match 401k
- Reasonable accommodations during the employment application process