Review advertising, website content, product pages, packaging, social media, and sales materials to ensure clinical and performance claims are accurate, substantiated, and compliant.
Evaluate supporting evidence (clinical studies, published literature, consumer research) to determine its strength for backing each claim.
Partner with Marketing, Legal, Regulatory, Clinical, and Product teams to provide clear guidance on claim wording, risk level, and additional substantiation.
Lead advertising review process improvements and develop scalable workflows for compliance.
Review advertising and promotional claims across multiple channels for FDA, FTC, and consumer protection compliance.
Partner with Growth, Creative, and Clinical teams to streamline reviews and support timely campaign launches.
Ro is a direct-to-patient healthcare company offering nationwide telehealth, labs, and pharmacy services. It has helped millions of patients since 2017 and is recognized as a top workplace in healthcare and New York.
Review all customer-facing marketing materials to ensure compliance with legal and regulatory guidelines.
Serve as a partner to cross-functional teams, providing guidance on compliant messaging and exercising judgment on escalations.
Lead documentation of best practices and develop an intake system for marketing review requests.
Hims & Hers is a leading health and wellness platform on a mission to help people feel great through better health. As a public company traded on NYSE (HIMS), they prioritize customer-first personalized care and offer a talent-first remote work culture.
Analyze high-value and complex claims, ensuring alignment with carrier guidelines and regulatory requirements.
Oversee delegated claims operations and third-party administrators, monitoring compliance and quality.
Provide subject matter expertise and process improvements to strengthen claims governance and outcomes.
They are an insurance organization focused on claims governance, compliance, and operational performance. They are a growing company that prioritizes accountability, service quality, and effective risk management.
Execute regulatory oversight for advertising, promotion, medical communications, and labeling across the product lifecycle.
Provide proactive regulatory strategy and risk-based guidance to commercial and medical review committees.
Lead FDA OPDP/APLB interactions and cross-functional labeling negotiations with health authorities.
Kyverna Therapeutics is a biopharmaceutical company developing cell therapies for autoimmune diseases. It is a growth-stage biotech with a collaborative, solutions-oriented culture and a focus on regulatory excellence.
Coordinate end-to-end review and approval of promotional, advertising, and commercial materials in a regulated life sciences environment.
Serve as central point of contact for internal teams and external partners, managing documentation, timelines, and approval records.
Work closely with Regulatory Affairs, Legal, Medical, Compliance, Marketing, and Commercial stakeholders to ensure efficient and compliant reviews.
A growing life sciences organization dedicated to advancing regenerative medicine through innovative products and high-quality solutions. The company fosters a collaborative culture focused on accountability, adaptability, continuous learning, and customer-centric innovation.