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Revisto

MLR Review Specialist

Reposted 7 Days Ago
Be an Early Applicant
Remote
Hiring Remotely in United States
Expert/Leader
Remote
Hiring Remotely in United States
Expert/Leader
Reviews pharmaceutical promotional materials for medical, legal, and regulatory compliance; creates evidence-based claims; evaluates AI outputs; applies FDA and EMA requirements; and collaborates with product, engineering, and client MLR teams to improve platform accuracy, workflows, and compliance. Serves as an internal subject matter expert and helps guide product development and client success.
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About Us

At Revisto, we’re revolutionizing the pharmaceutical industry by streamlining the medical, legal, and regulatory (MLR) review process with cutting-edge AI technology. Based in the vibrant tech hub of Austin, Texas, our rapidly growing startup—recently bolstered by $6 million in funding, including a $4 million seed round by LiveOak Ventures, Arkin Capital, and Tau Ventures, and backed by industry giants like Eli Lilly—empowers life sciences companies to bring marketing materials to market faster, smarter, and with uncompromising compliance. Our AI-driven platform automates tedious review cycles, saving millions in costs and unlocking data-driven, personalized marketing that drives positive patient outcomes. Join our dynamic team of innovators and industry experts as we scale to transform pharmaceutical marketing worldwide.

Role Overview

We’re seeking a passionate MLR Review Specialist to be part of our leadership team and join our mission of delivering best-in-class, compliant promotional materials through our innovative AI platform. You’ll play a key role in optimizing our industry-leading AI system by providing expert validation, refining its performance, and ensuring seamless alignment with client workflows. Leveraging your expertise and understanding of tools like Veeva Vault PromoMats, you’ll help shape the future of our platform as we scale to meet the needs of the global life sciences industry.

Key Responsibilities
  • Expert Validation: Evaluate promotional materials processed by our advanced AI platform to confirm outputs meet medical, legal, and regulatory standards (e.g., FDA, EMA), ensuring our system consistently delivers compliant results

  • Claim Creation: Craft evidence-based, compliant claims from clinical trial reports, scientific literature, and other reference materials to support platform enhancements and client needs.

  • Regulatory Expertise: Stay ahead of evolving global and local regulations in pharmaceutical marketing, applying your knowledge to keep our platform and processes at the forefront of compliance.

  • Quality Assurance: Conduct periodic evaluations of AI outputs to validate performance, identifying opportunities to further refine accuracy and efficiency

  • Platform Enhancement: Collaborate with our product and engineering teams, using insights from customer materials and your expertise to drive continuous improvements to our AI platform.

  • Client Partnership: Engage with MLR experts at client organizations to understand their workflows, gather feedback, and ensure our platform integrates seamlessly with their processes

  • Knowledge Leadership: Share MLR best practices with internal teams, guiding product development and client success as a subject matter expert.

Qualifications
  • Education: Advanced degree in medicine, pharmacy, life sciences, or a related field. Additional training in regulatory affairs or pharmaceutical marketing is a plus.

  • Experience:

    • 7–10 years in MLR review, regulatory affairs, or pharmaceutical marketing, with hands-on experience reviewing promotional materials and creating claims, ideally across multiple leading pharmaceutical companies.

    • Strong understanding of compliance standards across medical, legal, and regulatory domains.

    • Hands-on experience with Veeva Vault PromoMats in MLR review workflows.

    • Proven ability to collaborate with MLR experts or stakeholders in client-facing roles.

  • Mindset & Attributes:

    • Go-getter mentality with a proactive, entrepreneurial spirit, eager to take initiative and drive impact in a fast-paced startup environment.

    • Eagerness to learn new things and try new approaches, with a curiosity to innovate and adapt in a dynamic, tech-driven setting.

  • Expertise & Skills:

    • Deep expertise in MLR reviews, with a keen eye for ensuring compliance in promotional content..

    • Proficiency in generating compliant claims from scientific literature and clinical data.

    • Knowledge of global regulatory frameworks (e.g., FDA, EMA) for claim substantiation.

    • Strong analytical skills to evaluate AI outputs against human expertise.

    • Exceptional attention to detail and commitment to excellence.

  • Communication: Ability to clearly articulate findings and recommendations to technical and non-technical audiences, and build strong relationships with client MLR experts.

  • Tech Savvy: Enthusiasm for working with AI-driven tools and thriving in a technology-forward environment.

Preferred Skills
  • Experience with AI or software-driven solutions in the pharmaceutical industry.

  • Ability to translate MLR expertise into actionable improvements for technology platforms.

  • Comfort managing multiple priorities in a dynamic, growth-oriented startup environment.

Join Revisto and be part of a fast-growing team that’s transforming pharmaceutical marketing with AI innovation. Apply today to help us shape the future of personalized marketing in life sciences!

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