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Cytokinetics
Director, US Regulatory Affairs, Advertising & Promotion
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What they do
A Regulatory Affairs Manager plans, directs, or coordinates production activities of an organization to ensure compliance with regulations and standard operating procedures.
$235,442 / year median in California
-1% projected decline
Job Description
Director, US Regulatory Affairs, Advertising & Promotion Cytokinetics - 4.3 San Francisco, CA Job Details Full-time $225,000 - $262,500 a year 2 hours ago Benefits Stock options Disability insurance Health insurance Dental insurance RSU Paid time off Vision insurance 401(k) matching Qualifications FDA submissions Drug regulation Bachelor's degree Pharmaceutical company experience Legal compliance Full Job Description Cytokinetics is a specialty cardiovascular biopharmaceutical company, building on its over 25 years of pioneering scientific innovations in muscle biology, and advancing a pipeline of potential new medicines for patients suffering from diseases of cardiac muscle dysfunction. The Director Regulatory Affairs, Advertising and Promotion plays a critical role in providing strategic regulatory leadership and oversight for commercial, promotional, and medical communications. This role ensures that marketing campaigns, disease awareness initiatives, and corporate communications comply with FDA regulations, and company policies. Operating with a high degree of autonomy, the Director collaborates with clinical, medical, and legal to serve as a bridge between commercial tactics and regulatory compliance. Key Responsibilities US Regulatory Review & Compliance Lead regulatory review and approval of U.S. product promotional materials. Ensure product claims are supported by FDA-approved labeling and are scientifically substantiated Serve as the regulatory advertising and promotion subject matter expert for the organization Influence cross-functional decision making through strategic regulatory guidance. Mentor junior regulatory professionals and contribute to talent development initiatives Lead continuous improvement efforts related to promotional review processes and governance Represent regulatory on the MLR Committee, and provide strategic regulatory input during new concept reviews, and review and approve materials for regulatory compliance Review non-promotional assets, including medical, corporate affairs, market access/payor communications, and patient advocacy materials Develop and update Important Safety Information (ISI) and risk presentations for use in commercial assets for target audiences FDA Liaison & Submissions Lead regulatory strategy for OPDP interactions, including advisory comments, enforcement responses, and regulatory correspondence as appropriate Manage FDA Form 2253 submissions for applicable commercial assets Lead voluntary advisory comment submissions for identified materials Corporate Readiness & Training Monitor OPDP enforcement trends and FDA guidance documents, and communicate relevant updates and learnings with cross functional stakeholders Create or update standard operating procedures (SOPs) or work instructions to optimize and streamline work processes Train U.S. marketing, sales, and medical affairs teams on regulatory compliance