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Centene

Senior Manager, Medical Loss Ratio

Columbia, MO · On-site +1

Accountable for the Medical Loss Ratio (MLR) compliance and reporting program across assigned lines of business, ensuring accurate calculation, strong governance and controls, and timely submission ...

Praxis Precision Medicines, Inc.

CMLR Coordinator

OR · On-site +1

Coordinate end-to-end MLR review workflows for promotional, educational, and corporate materials across multiple functions and stakeholders * Manage review timelines, approvals, version control ...

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How much do mlr jobs pay per year?

As of Aug 6, 2026, the average yearly pay for mlr in the United States is $65,245.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,000.00 and $84,000.00 per year, depending on experience, location, and employer.

What is an MLR?

An MLR (Medical, Legal, and Regulatory) job typically involves reviewing and approving marketing and promotional materials in industries like pharmaceuticals and healthcare. Professionals in this role ensure that content complies with regulatory standards, company policies, and legal requirements. They work closely with cross-functional teams, including medical affairs, compliance, and marketing, to mitigate risks and maintain ethical standards.

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To excel as a Machine Learning Researcher (MLR), you should have a solid background in computer science, mathematics, and statistics, typically with an advanced degree in a related field. Experience with programming languages such as Python or R, proficiency in machine learning frameworks like TensorFlow or PyTorch, and knowledge of data processing tools are commonly required. Strong analytical thinking, curiosity, and the ability to communicate complex ideas clearly distinguish top candidates. These skills enable MLRs to develop innovative models, interpret results, and collaborate effectively in interdisciplinary research teams.

What are the typical daily responsibilities of a machine learning researcher?

Machine Learning Researchers typically spend their days designing and developing new algorithms, running experiments on large datasets, and analyzing model performance to refine their approaches. They often collaborate closely with data scientists, engineers, and domain experts to translate theoretical findings into practical applications. Literature review and staying current with recent advancements in the field are also important routine activities. This role balances independent research with teamwork, contributing to innovative projects that push the boundaries of what machine learning can achieve.

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Mlr jobs near you
Infographic showing various Mlr job openings in the United States as of August 2026, with employment types broken down into 90% Full Time, 1% Part Time, 1% Temporary, and 8% Contract. Highlights an 65% Physical, 10% Hybrid, and 25% Remote job distribution, with an average salary of $65,245 per year, or $31.4 per hour.

Medical, Legal & Regulatory (MLR) Specialist

Cristcot

Remote

Full-time

Re-posted 6 days ago

Job description

About Cristcot
We are in the business of addressing the problem within the problem. We focus on the details and connections that other, major pharma companies have left ignored for years. There are better ways, better drugs and better formulations and we will make them a reality by analyzing, understanding and solving the problems within the problems.
Job Summary
We are seeking a highly organized and accountable MLR Specialist for the operational management, coordination, and continuous improvement of the Medical, Legal, and Regulatory (MLR) review process across Marketing, Medical Affairs, and Corporate Communications. This role serves as a central point of coordination for promotional review activities, ensuring materials are reviewed, approved, documented, and archived in accordance with FDA regulations, company policies, and industry best practices.
Primary Relationships:
  • Within Cristcot: The MLR Specialist will partner cross-functionally with Medical Affairs, Regulatory Affairs, Legal, Compliance, Commercial, and Marketing.
  • Outside Cristcot: The MLR Specialist will collaborate with external agency partners to ensure materials are reviewed efficiently, compliantly, and within established timelines.

Primary Job Responsibilities
The position partners closely with cross-functional stakeholders, including Marketing, Medical Affairs, Regulatory Affairs, Legal, Compliance, Corporate Communications, external agencies, and content management teams to facilitate efficient review workflows, maintain compliance documentation, support audit readiness, and drive process optimization initiatives.
The activities of the MLR Specialist will include, but are not limited to:
Promotional Review Operations
  • Oversee and manage MLR review and approval submissions for Marketing, Medical Affairs, and Corporate Communications materials.
  • Partner with Medical Affairs teams to ensure appropriate submission ownership and coordination of review materials.
  • Coordinate MLR review meetings and ensure timely routing of materials to designated reviewers.
  • Maintain and manage the Master MLR Review Schedule across all business functions.
  • Develop, maintain, and communicate a weekly MLR "Hot Sheet" highlighting all active and upcoming review activities requiring approval.
  • Track review status, approvals, reviewer comments, revision cycles, and final disposition of materials.
  • Collaborate with agencies, content creators, and internal library resources to ensure supporting references, journal articles, and documentation are appropriately maintained within Zotero and related content repositories.
  • Partner with leadership to identify workflow efficiencies and recommend process improvements to enhance review timelines and stakeholder experience.

Compliance Documentation & Systems Management
  • Maintain promotional review systems, approval workflows, records, and documentation repositories.
  • Ensure proper version control and archival of approved materials and supporting documentation.
  • Maintain audit-ready records for all promotional review activities and approvals.
  • Manage tracking systems for FDA submissions, OPDP correspondence, advisory comments, approval records, version histories and compliance documentation
  • Ensure approved content is accurately maintained across applicable content management platforms and repositories.
  • Coordinate updates and maintenance activities to ensure content is current and compliant.
  • Support licensing and access management for content review platforms, including Vodori, Veeva, and related systems.

Process Management & Compliance Oversight
  • Ensure promotional and communication materials adhere to FDA regulations, industry guidelines, company policies, and applicable compliance standards.
  • Monitor review timelines and identify bottlenecks or process gaps affecting review efficiency.
  • Partner with leadership to implement corrective actions and workflow enhancements.
  • Generate and distribute MLR metrics, dashboards, and reporting to support business and compliance objectives.
  • Assist in the development, revision, and maintenance of Standard Operating Procedures (SOPs), work instructions, and training documentation.
  • Conduct training sessions for internal teams, external agencies, and business partners on promotional compliance requirements and MLR best practices.
  • Drive status reporting, risk identification, and issue resolution activities to keep leadership informed and key launch initiatives on track.
  • Work with management to define, document, and continuously improve Promotional Review Committee (PRC) processes, including submission workflows, review timelines, approval pathways, escalation protocols
  • Monitor FDA guidance, enforcement actions, and industry trends to proactively recommend adjustments to communication and review practices.

Skills and Qualifications
  • Bachelor's degree in Life Sciences, Business, Marketing, Communications, Healthcare Administration, or a related field.
  • 3-7+ years of experience supporting MLR/PRC operations, promotional review, regulatory operations, compliance, or pharmaceutical marketing processes.
  • Working knowledge of FDA promotional regulations, OPDP requirements, and pharmaceutical industry compliance standards.
  • Experience with promotional review systems such as Veeva PromoMats, Vodori, or similar platforms.
  • Strong project management, organizational, and coordination skills.
  • Excellent attention to detail and documentation management capabilities.
  • Ability to manage multiple projects simultaneously in a fast-paced environment.
  • Strong communication, collaboration, and stakeholder management skills.
  • Experience supporting Medical Affairs, Commercial, and Corporate Communications review processes preferred.
  • Knowledge of content management systems, reference libraries, and citation management tools such as Zotero preferred.
  • Experience developing compliance metrics, dashboards, and reporting preferred.
  • Familiarity with audit readiness and inspection support activities preferred.
  • Project management certification or formal process improvement training is a plus.
  • Ability to support meetings across multiple U.S. time zones.
  • May require occasional travel for team meetings, launch activities, or training.
Cristcot logo

About Cristcot

Sourced by ZipRecruiter

Industry

Medical equipment and supplies manufacturing

Company size

11 - 50 Employees

Headquarters location

Concord, MA, US

Year founded

2008

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