Associate Manager, Clinical Claims

Posted Yesterday
Easy Apply
Be an Early Applicant
2 Locations
In-Office or Remote
109K-136K Annually
Mid level
Healthtech • Pharmaceutical • Telehealth
Ro's mission is to help patients achieve their health goals by delivering the easiest, most effective care possible.
The Role
Reviews and substantiates clinical, performance, advertising, and promotional claims across Ro’s marketing channels. Evaluates clinical studies, literature, and consumer research for evidentiary strength and regulatory compliance. Partners with Marketing, Legal, Regulatory, Clinical, and Product teams on claim wording and risk. Builds the claims library, evidence database, review processes, templates, and approval workflows while providing practical, defensible guidance.
Summary Generated by Built In
Ro is a direct-to-patient healthcare company with a mission of helping patients achieve their health goals by delivering the easiest, most effective care possible. Ro is the only company to offer nationwide telehealth, labs, and pharmacy services. This is enabled by Ro's vertically integrated platform that helps patients achieve their goals through a convenient, end-to-end healthcare experience spanning from diagnosis, to delivery of medication, to ongoing care. Since 2017, Ro has helped millions of patients in nearly every single county in the United States, including 99% of primary care deserts.
 
Ro is consistently recognized as a top workplace in Health Care, in New York, and for Women and Parents—earning more than 20 honors from Fortune, Great Place to Work, and PEOPLE since 2021. In 2025 alone, we ranked top 5 among medium workplaces in Health Care and New York, and top 50 nationwide.

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

The target base salary for this position ranges from $109,200 to $136,000, in addition to a competitive equity and benefits package (as applicable). When determining compensation, we analyze and carefully consider several factors, including location, job-related knowledge, skills and experience. These considerations may cause your compensation to vary.

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 [email protected].
 
See our California Privacy Policy here.

Skills Required

  • 3–5 years of experience in claims substantiation, medical-legal-regulatory review, advertising and promotion regulatory affairs, clinical research, or a related field
  • Ability to critically appraise clinical data, including study design, sample size, endpoints, and statistical versus clinical significance
  • Working knowledge of FDA and FTC advertising and labeling standards, including structure/function and disease claims
  • Experience partnering with Marketing and Legal in a review or approval process
  • Excellent written and verbal communication skills, including translating technical findings for non-scientific audiences
  • Bachelor’s degree in a scientific or health-related field
  • Advanced degree
  • Consulting experience in regulatory, advertising compliance, or life sciences advisory
  • Experience with NAD challenges or regulatory inquiries
  • Experience building a claims review function from the ground up

What the Team is Saying

Kim
Rachel
Andres
Ross
Kerry
Jay
Zach
Am I A Good Fit?
beta
Get Personalized Job Insights.
Our AI-powered fit analysis compares your resume with a job listing so you know if your skills & experience align.

The Company
HQ: New York, NY
824 Employees
Year Founded: 2017

What We Do

Ro is a direct-to-patient healthcare company with a mission of helping patients achieve their health goals by delivering the easiest, most effective care possible. Ro is the only company to offer nationwide telehealth, labs, and pharmacy services. This is enabled by Ro's vertically integrated platform that helps patients achieve their goals through a convenient, end-to-end healthcare experience spanning from diagnosis, to delivery of medication, to ongoing care. Since 2017, Ro has helped millions of patients in nearly every single county in the United States, including 98% of primary care deserts.

Why Work With Us

Ro is powering quality care at scale. The Ro Operating System (ro.OS) vertically integrates the core parts of healthcare, bringing together nationwide telehealth, lab, and pharmacy services on one platform. The result? ro.OS makes it easier for patients to access and providers to deliver high-quality care – millions of times over.

Gallery

Gallery
Gallery
Gallery
Gallery
Gallery
Gallery

Ro (Ro.co) Teams

Team
Technology
Team
Clinical
Team
Pharmacy
About our Teams

Ro (Ro.co) Offices

Hybrid Workspace

Employees engage in a combination of remote and on-site work.

Ro’ers in the tri-state area join their colleagues in the NY Hub twice a week for in-person collaboration.

Typical time on-site: 2 days a week
HQRo HQ
US
Learn more

Similar Jobs

Ro (Ro.co) Logo Ro (Ro.co)

Principal Product Designer

Healthtech • Pharmaceutical • Telehealth
Easy Apply
In-Office or Remote
2 Locations
824 Employees
242K-285K Annually

Ro (Ro.co) Logo Ro (Ro.co)

Editor

Healthtech • Pharmaceutical • Telehealth
Easy Apply
In-Office or Remote
2 Locations
824 Employees
112K-133K Annually

Ro (Ro.co) Logo Ro (Ro.co)

Operations Manager

Healthtech • Pharmaceutical • Telehealth
Easy Apply
Remote or Hybrid
2 Locations
824 Employees
109K-143K Annually

Ro (Ro.co) Logo Ro (Ro.co)

Manager, Practice Operations

Healthtech • Pharmaceutical • Telehealth
Easy Apply
In-Office or Remote
2 Locations
824 Employees
102K-125K Annually

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account