Content Compliance Manager

#LI-HybridThe Content Compliance Manager role sits at the center of how trusted, compliant content comes to life-where strategy, execution, and partnership intersect. As a Content Compliance Manager, you'll own the end-to-end stewardship of commercial content, working closely with Brand, Medical, Legal, Regulatory, and agency partners to enable confident decisions, reduce risk, and bring predictability to the content lifecycle. If you're motivated by ownership, impact, and building disciplined, modern ways of working that truly matter, this is a role where your influence will be seen and felt.This position will be located in East Hanover, NJ and will not have the ability to be located remotely. Relocation may be possible and requires necessary approvals.Key Responsibilities:Own end‑to‑end MAP execution from intake through approval, distribution, maintenance, and withdrawal.Lead MAP submissions across brands and functions, including Urgent PR, Market Access, Training, Communications, and Patient Services.Validate submission readiness, metadata accuracy, and reviewer routing aligned to MAP governance and triage standards.Anticipate and manage risks, delays, and dependencies through forecasting, communication, and cross‑functional collaboration.Ensure in‑market compliance by managing asset expiration, withdrawal, and documentation in DAM and downstream systems.Partner with Content Owners to ensure timely asset removal aligned to expiration, withdrawal, or label changes.Contribute to MAP forecasting and capacity planning to improve demand visibility and reduce unplanned work.Govern consistent use of MAP and DAM tools, troubleshooting issues and enabling standardized ways of working.Serve as a trusted cross‑functional partner, clearly communicating status, risks, options, and recommendations.Essential Requirements:Bachelor's degree required; major in Business, Marketing, Communications, or related discipline preferred3+ years of experience in pharmaceutical advertising, marketing operations, content, or communicationsWorking knowledge of FDA and pharmaceutical promotional regulations and compliance principlesFamiliarity with pharmaceutical review and approval processes (MAP or equivalent)Strong project and workflow management skillsAbility to use data, systems, and structured methodologies to manage work and inform decisionsProficiency with Microsoft 365 and content review / DAM systems (e.g., Aprimo or similar preferred, PowerPoint, and Excel)Clear communicator with strong organizational skills and attention to detailNovartis Compensation Summary:The salary for this position is expected to range between $108,500 and $201,500 per year.The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.