Associate Manager, Clinical Claims
At a glance
Manager-level role at Ro. Remote, United States · full-time · $109,200–$136,000 base.
remoteroles summary, based on the employer's posting.
What you'll do
- Check claims in ads, web pages, packaging, social posts and sales materials for accuracy, evidence and compliance
- Assess studies, published research and consumer findings to decide whether they support each claim
- Advise partner teams on wording, risk and evidence gaps, offering viable alternatives for marketing
- Maintain the approved-claims library and supporting evidence database so decisions can be traced
- Build review templates and approval steps, then audit priority claims and propose process improvements
What you bring
- Three to five years in claims substantiation, MLR review, promotion regulation, clinical research or a related area
- You can judge study design, sample size, endpoints and the difference between statistical and clinical significance
- You understand FDA and FTC rules for advertising and labeling, including structure/function versus disease claims
- You have partnered with marketing and legal teams on reviews, and hold a bachelor’s degree in a scientific or health field
Who this fits
This role suits a scientifically rigorous communicator who can turn clinical findings into usable guidance for non-scientific teams. The position is remote across the United States; employees in the New York tri-state area attend HQ on Tuesdays and Thursdays, while others may join in-person team sessions during the year.
From the employer
The Role:
As an Associate Manager, Clinical Claims, you’ll make sure everything Ro says about its products and services is accurate, evidence-based, and compliant, while helping Marketing say it boldly and defensibly. You’ll review advertising and broader company claims across channels, partnering closely with Marketing, Legal, Regulatory, Clinical, and Product teams and reporting to the Director of Scientific Affairs. You’re a rigorous, curious scientific thinker who can translate complex clinical data into clear, practical guidance. You’ll have the chance to build and own the claims framework, review process, and evidence library as Ro scales.
What You’ll Do:
- 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) and determine whether it is strong enough to support each claim
- Partner with Marketing, Legal, Regulatory, Clinical, and Product to give clear guidance on claim wording, risk level, and any additional substantiation needed
- Enable bold, defensible marketing by offering workable alternatives and solutions
- Own and build the claims library and evidence database so approved claims and their supporting data are documented and defensible
- Establish and refine claims review processes, templates, and approval workflows that scale with the business
- Success in your first 90 days: learn the portfolio and current review process, audit high-visibility and high-risk claims in market, build relationships with key stakeholders, and propose a prioritized roadmap for process improvements and claims library buildout
What You’ll Bring to the Team:
- 3 - 5 years of experience in claims substantiation, medical-legal-regulatory (MLR) review, advertising and promotion regulatory affairs, clinical research, or a related field
- Strong ability to critically appraise clinical data, including study design, sample size, endpoints, and statistical vs. clinical significance
- Working knowledge of FDA and FTC advertising and labeling standards, including the distinction between structure/function and disease claims
- Proven experience partnering with Marketing and Legal in a review or approval process
- Excellent written and verbal communication, with the ability to translate technical findings into clear, practical guidance for non-scientific audiences
- Bachelor’s degree in a scientific or health-related field (advanced degree a plus)
- Bonus points for consulting experience (regulatory, advertising compliance, or life sciences advisory), experience with NAD challenges or regulatory inquiries, or experience building a claims review function from the ground up
We’ve Got You Covered:
- Full medical, dental, and vision insurance + OneMedical membership
- Healthcare and Dependent Care FSA
- 401(k) with company match
- Flexible PTO
- Wellbeing + Learning & Growth reimbursements
- Paid parental leave + Fertility benefits
- Pet insurance
- Student loan refinancing
- Virtual resources for mindfulness, counseling, and fitness
Ro recognizes the power of in-person collaboration, while supporting the flexibility to work anywhere in the United States. For our Ro’ers in the tri-state (NY) area, you will join us at HQ on Tuesdays and Thursdays. For those outside of the tri-state area, you will be able to join in-person collaborations throughout the year (i.e., during team on-sites). At Ro, we believe that our diverse perspectives are our biggest strengths — and that embracing them will create real change in healthcare. As an equal opportunity employer, we provide equal opportunity in all aspects of employment, including recruiting, hiring, compensation, training and promotion, termination, and any other terms and conditions of employment without regard to race, ethnicity, color, religion, sex, sexual orientation, gender identity, gender expression, familial status, age, disability and/or any other legally protected classification protected by federal, state, or local law. Ro is committed to providing reasonable accommodations for qualified individuals with disabilities in our application and interview process. If you require a reasonable accommodation in the application or interview process, please contact us at talent@ro.co. See our California Privacy Policy here.