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.
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.
Serve as the Legal representative on the Promotional Review Committee and Medical Review Committee, reviewing HCP-facing, patient-facing, medical, and corporate materials for compliance with FDA regulations and industry codes.
Provide practical legal guidance across pre-launch and launch activities, including patient education, digital content, and patient support programs, balancing legal risk with business objectives.
Review non-promotional materials, evaluate claims for substantiation, and advise on compliantly navigating the regulatory landscape for digital, social, and medical affairs content.
Mineralys Therapeutics is a clinical-stage biopharmaceutical company focused on developing medicines to target hypertension and related comorbidities such as chronic kidney disease, obstructive sleep apnea, and other diseases driven by dysregulated aldosterone. Headquartered in Radnor, Pennsylvania, Mineralys is a fully remote company with a collaborative, fast-moving culture.
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.
Serve as the primary compliance point of contact for strategic partnerships and clients.
Lead the compliance workstream for major brand migrations and become an expert on the Regulated Compliance product.
Monitor compliance processes, ensure accurate documentation, and deliver presentations on compliance matters.
impact.com is the world's leading commerce partnership marketing platform, helping brands manage partnerships with affiliates, influencers, and creators. With over 5,000 global brands relying on the platform, the company fosters a flexible, performance-driven culture.
Ensure marketing, educational, and communications materials comply with FDA, FTC, USP, and state pharmacy regulations.
Lead cross-functional content reviews and provide practical, risk-based compliance guidance to teams.
Develop compliance SOPs, training resources, and auditable documentation to support scalable content operations.
Strive Pharmacy is a personalized compounding pharmacy that creates custom medications tailored to individual patient needs. The company is a growing team focused on disrupting the pharmaceutical industry with a human-centered approach and a collaborative culture.
Lead advanced compliance activities for healthcare administrative products including HSAs, FSAs, HRAs, and COBRA.
Apply expert regulatory judgment to risk assessments, compliance monitoring, investigations, and corrective actions.
Collaborate with stakeholders to integrate compliance requirements into strategic initiatives and leverage AI-powered tools.
HealthEquity empowers healthcare consumers by providing administrative solutions like HSAs, HRAs, FSAs, and COBRA. The company is a large, mission-driven organization that values inclusion and connects health and wealth for American families.
Own the AI marketing review tool and drive automation of compliance reviews.
Manage end-to-end marketing compliance review process, standards, and recordkeeping.
Serve as player-coach, handling reviews and building the team's capabilities.
Ethos is a life insurance technology company using a three-sided platform to transform how life insurance is bought, sold, and underwritten. It focuses on making coverage accessible with no medical exams and fostering a diverse, inclusive workplace.
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.
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.
Develops and drives regulatory strategy for FDA Pharma and IVDR initiatives.
Represents the regulatory function on cross-functional teams and interacts with regulatory authorities.
Coordinates regulatory submissions and ensures compliance with global requirements.
Natera is a clinical genetic testing company specializing in non-invasive cell-free DNA and liquid biopsy testing. The team consists of highly dedicated professionals from world-class institutions who care deeply for their work and each other.
Social Discovery Group creates social entertainment platforms that connect people online across cultures and regions. The international remote team is recognized as a Great Place to Work (USA & Japan, 2024–2025) and a Top-5 Company for Work-From-Anywhere Jobs.
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.
Set the strategic direction and long-term roadmap for Extend's regulatory compliance program, spanning licensing, service contracts, and insurance.
Serve as the executive-level owner for regulatory and licensing matters, representing compliance in front of regulators and auditors.
Partner with cross-functional teams to embed compliance requirements into merchant onboarding, customer experience, and product workflows.
Extend provides AI-driven solutions for retailers to enhance post-purchase customer satisfaction and drive revenue growth. The company works with more than 1,000 merchant partners, is backed by prominent technology investors, and is headquartered in downtown San Francisco.
Build trust with state healthcare regulatory boards and agencies to drive growth of the CE Broker solution.
Serve as the primary point of contact for assigned state partners, guiding operational efficiency and compliance.
Navigate multi-year government decision cycles with a consultative, relationship-first approach.
Propelus simplifies workforce compliance management across healthcare, providing technology and strategic partnerships that empower professionals, employers, and regulators. A trusted leader for over 20 years, the company serves millions with seamless compliance solutions and has been named a BuiltIn 2025 Best Places to Work.
Review product specifications and mobile app features to ensure compliance with legal and platform requirements.
Advise marketing teams on EU and US advertising regulations, consumer protection, and promotional claims.
Monitor regulatory developments, including AI governance and sanctions, and support compliance training and risk assessments.
Our partner is an international, remote-first organization developing innovative digital products that help people build meaningful connections across cultures and communities. They have a globally distributed team of technology professionals working collaboratively across different markets.
Manage marketing operations workflows including creative asset updates, tagging, disclosures, and content administration across platforms.
Coordinate project timelines, stakeholder approvals, and regulatory compliance across marketing, legal, and compliance teams.
Independently drive smaller tactical marketing projects from intake to completion while maintaining audit-ready documentation.
This partner company is a leading organization in the digital payments and financial services industry. The team supports a remote consulting environment with a focus on collaboration, diversity, and inclusion.
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.
Draft and negotiate advertising and ad tech agreements, including supply-side, demand-side, and content licensing deals.
Collaborate with privacy and product attorneys to ensure ad transactions comply with CCPA, GDPR, and related laws.
Build templates, playbooks, and workflows to accelerate deal closure while protecting the company.
Life360 keeps people close to loved ones through its mobile app, Tile trackers, and Pet GPS. With 500+ remote-first employees and 102M+ monthly active users, it fosters a mission-driven, belonging-focused culture.