ZipRecruiter

Log In

1

Mlr Review Jobs (NOW HIRING)

Avery Healthcare Group Ltd.

Falcon MLR Strategy - EU

$56.50 - $73/hr

The Role MLR review is one of the Life Science industry's biggest bottlenecks - and we're rebuilding it with AI. Falcon MLR is Veeva's AI application for medical, legal, and regulatory (MLR) review.

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 ...

Praxis Precision Medicines, Inc.

CMLR Coordinator

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

Prophecy Technologies

Veeva Technical Architect

Raritan, NJ · On-site

$64.50 - $85/hr

Serve as the primary technical advisor for PromoMats capabilities including Digital Asset Management (DAM), MLR Review Process, Claims Management, Content Lifecycle Management, Modular Content ...

Jobtailor

Director, Medical Communications

Cary, NC · On-site

$120 - $180/hr

Oversee Medical Affairs website and content hub strategy, including content planning, taxonomy/SEO, asset readiness, MLR review coordination, and user-experience input * Integrate new assets ...

Astrazeneca

MLR Planning Manager

Gaithersburg, MD

$151K - $226K/yr

MLR Planning Manager Location: Gaithersburg, MD Introduction to role: Are you ready to orchestrate ... Can you align brand priorities with reviewer capacity to hit critical dates without sacrificing ...

next page

Showing results 1-20

All JobsHealthcare JobsHospital JobsMedical Reviewer JobsMlr Review Jobs

Mlr Review information

See salary details

$35K

$65.2K

$116.5K

How much do mlr review jobs pay per year?

As of Aug 24, 2026, the average yearly pay for mlr review 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 review?

MLR reviews, or Medical, Legal, and Regulatory reviews, are processes in which promotional and scientific materials are evaluated to ensure they comply with industry regulations, company policies, and relevant laws. These reviews are commonly conducted in the pharmaceutical, biotech, and medical device industries. The MLR review process typically involves collaboration among medical, legal, and regulatory professionals who assess materials for accuracy, balance, and compliance before they are released to the public or healthcare professionals. The goal is to ensure that all information is truthful, not misleading, and adheres to regulatory standards.

What skills and qualifications are needed to thrive as an MLR reviewer?

To thrive as an MLR Reviewer, you need a strong background in medical writing, regulatory compliance, and a solid understanding of pharmaceutical or healthcare industry standards, often supported by relevant degrees or certifications. Familiarity with tools such as document management systems, regulatory databases, and compliance tracking software is typically required. Attention to detail, critical thinking, and effective communication are crucial soft skills for collaborating with cross-functional teams and ensuring accuracy. These skills are essential for maintaining compliance, reducing risk, and ensuring that all promotional and scientific materials meet legal and regulatory requirements.

How does an MLR review professional collaborate with cross-functional teams during the content review process?

As an MLR (Medical, Legal, and Regulatory) Review professional, you will work closely with teams from medical, legal, regulatory, and marketing departments to ensure all promotional and educational materials meet compliance standards. Effective communication and attention to detail are crucial, as you will often participate in review meetings, provide feedback, and help resolve any discrepancies to align materials with industry regulations and company policies. This collaborative environment fosters continuous learning and exposes you to diverse perspectives, which can support your professional growth within the organization.

What is the difference between Mlr Review vs Data Analyst?

AspectMlr ReviewData Analyst
Required CredentialsTypically requires knowledge of machine learning, data analysis, and relevant certificationsRequires statistical, analytical, and often programming skills, with degrees in related fields
Work EnvironmentOften involves reviewing machine learning models, algorithms, and data processesAnalyzing data sets, creating reports, and providing insights for business decisions
Industry UsageCommon in AI, machine learning, and data science companiesUsed across finance, marketing, healthcare, and tech industries

The comparison between Mlr Review and Data Analyst highlights differences mainly in focus and skill set. Mlr Review centers on evaluating machine learning models and algorithms, requiring specialized knowledge in AI and data science. Data Analysts focus on interpreting data, creating reports, and supporting decision-making across various industries. While both roles involve data, their core responsibilities and expertise areas differ significantly.

More about Mlr Review jobs

What cities are hiring for Mlr Review jobs?

Cities with the most Mlr Review job openings:

What states have the most Mlr Review jobs?

States with the most job openings for Mlr Review jobs include:

What job categories do people searching Mlr Review jobs look for?

The top searched job categories for Mlr Review jobs are:

Mlr Review jobs near you
Infographic showing various Mlr Review job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, 3% Contract, and 1% Nights. Highlights an 89% Physical, 3% Hybrid, and 8% 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 24 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

View All Cristcot Jobs

Apply