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 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.
Ro is a direct-to-patient healthcare company offering nationwide telehealth, labs, and pharmacy services. Since 2017, Ro has helped millions of patients and is recognized as a top workplace in Health Care, earning multiple honors from Fortune and Great Place to Work.
Serve as an internal subject matter expert on FTC and FDA advertising and marketing issues for health products.
Review and advise on product claims and substantiation including scientific studies, clinical data, and consumer perception research.
Collaborate with cross-functional teams to support new strategic initiatives and advertising campaigns.
Ro is a direct-to-patient healthcare company offering telehealth, labs, and pharmacy services through a vertically integrated platform. Since 2017, it has helped millions of patients across the US and is consistently recognized as a top workplace in health care, New York, and for women and parents.
Review advertising and promotional materials for FDA and FTC compliance, including websites, social media, TV spots, and billboards.
Collaborate with Legal and cross-functional teams to implement AI-enabled review workflows for efficiency and scalability.
Maintain company-wide guidelines and conduct trainings on advertising and promotion; stay current with FDA and FTC regulatory changes.
Ro is a direct-to-patient healthcare company that delivers telehealth, lab, and pharmacy services through a vertically integrated platform. Recognized as a top workplace in healthcare, New York, and for Women and Parents since 2021, it has earned multiple honors for its culture.
Provides strategic regulatory support and guidance for advertising and promotional communications for assigned product and disease state.
Serves as regulatory reviewer on Communications and Medical Review Committees, ensuring compliance with health authority regulations.
Collaborates with cross-functional teams to integrate regulatory requirements into promotional materials and conducts training sessions as needed.
Vertex Pharmaceuticals is a biotechnology company focused on developing transformative medicines for serious diseases, including cystic fibrosis and pain. The company is a large, established organization with a collaborative culture that values scientific innovation and regulatory compliance.
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.
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.
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.
Lead and supervise a team of regulatory specialists managing labeling approvals, drug listings, and medical device submissions.
Oversee FDA compliance, quality investigations, and health hazard evaluations to ensure product integrity.
Collaborate cross-functionally with Quality Assurance, Legal, and external partners to resolve complex regulatory challenges.
The partner company is a pharmaceutical and medical device organization focused on ensuring regulatory compliance and product quality. The company fosters a collaborative and inclusive work environment, emphasizing continuous improvement and professional development.
Write medically accurate, compelling copy for HCP, patient, and DTC pharma campaigns.
Translate complex clinical data into clear, on-brand messaging across digital, email, social, and more.
Partner with creative teams to develop integrated concepts while ensuring MLR compliance and brand voice.
Real Chemistry is a global healthcare communications and marketing agency combining deep scientific expertise, human-centred creativity, and AI-driven insights. Their #LifeatRealChem culture values collaboration, excellence, and impact, with teams across US offices and remote roles.
Provide professional regulatory consultancy to key retail clients, ensuring product safety and legal compliance.
Prepare and check pack copy, approve artwork, and ensure compliance with food labelling legislation.
Maintain technical competence and stay up to date with UK and EU legislation and industry trends.
SGS is the world's leading testing, inspection and certification company, recognized as a global benchmark for quality and integrity. With 100,000 employees across 2,600 offices and laboratories, we help ensure food safety, quality and compliance through our Food industry services.
Develop and implement global regulatory strategies for oncology programs from early development through post-marketing.
Lead preparation and submission of INDs, NDAs, and other regulatory filings to ensure compliance and quality.
Provide strategic regulatory guidance and cross-functional collaboration to drive program success.
Deciphera is a biopharmaceutical company focused on discovering, developing, and commercializing important new medicines for cancer, neurologic and autoimmune disease. They cultivate an inclusive culture that values curiosity, creativity, and shared accountability, empowering individuals to challenge the unknown together.
Lead the planning, authoring, and delivery of regulatory documents for global development programs, health authority interactions, and marketing applications.
Develop strategic document plans and author complex submissions such as INDs, CTAs, IBs, CSRs, and briefing packages while ensuring ICH/GCP compliance.
Coordinate cross-functional teams, manage external vendors, mentor junior writers, and drive process improvements to maintain submission readiness.
The company is a biopharmaceutical organization focused on developing innovative therapies for patients with significant unmet medical needs. It operates as a remote, cross-functional team with a culture emphasizing regulatory excellence, collaboration, and career development.