ZipRecruiter

Log In

1

Medical Content Review Jobs (NOW HIRING)

MJH Life Sciences

Principal Medical Writer

Cranbury, NJ · On-site

$95K - $105K/yr

Review and edit content at multiple stages for consistency, accuracy, relevance, and adherence to ... Medical Event Attendance: * Attend live events such as consensus meetings and professional ...

Inizio Engage

Hybrid Medical Writer

Titusville, NJ · On-site

$88K - $163K/yr

Create and/or co-create and review medical content for patients, HCPs and payers to ensure scientific rigor, balance and impact, this includes field medical slides (Medical Science Liaisons and ...

Inizio Engage

Hybrid Medical Writer

Titusville, NJ · On-site

$88K - $163K/yr

Create and/or co-create and review medical content for patients, HCPs and payers to ensure scientific rigor, balance and impact, this includes field medical slides (Medical Science Liaisons and ...

Inizio Engage

Hybrid Medical Writer

Yardley, PA · On-site

$88K - $163K/yr

Create and/or co-create and review medical content for patients, HCPs and payers to ensure scientific rigor, balance and impact, this includes field medical slides (Medical Science Liaisons and ...

Inizio

Hybrid Medical Writer

Princeton, NJ · Hybrid

$88K - $163K/yr

Create and/or co-create and review medical content for patients, HCPs and payers to ensure scientific rigor, balance and impact, this includes field medical slides (Medical Science Liaisons and ...

next page

Showing results 1-20

All JobsMedical Content Review Jobs

Medical Content Review information

See salary details

$15

$38

$77

How much do medical content review jobs pay per hour?

As of Jul 6, 2026, the average hourly pay for medical content review in the United States is $38.91, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $45.19 per hour, depending on experience, location, and employer.

What are some common challenges faced in a Medical Content Review role, and how can they be addressed?

One common challenge in Medical Content Review is ensuring accuracy and compliance with the latest medical guidelines while working within tight deadlines. Reviewers must stay up-to-date with constantly evolving regulations and scientific literature, which requires continuous learning and attention to detail. Effective collaboration with medical writers, subject matter experts, and legal teams can help address potential discrepancies or unclear messaging. Leveraging standardized checklists and clear communication channels also helps maintain quality and consistency across all reviewed content.

What is medical content review?

Medical content review is the process of evaluating medical or healthcare-related materials, such as articles, advertisements, or educational resources, to ensure they are accurate, compliant with regulations, and clear for the intended audience. Medical content reviewers check for scientific accuracy, proper use of medical terminology, and adherence to legal and ethical standards. This role is essential in maintaining the credibility and safety of information distributed to healthcare professionals and the public.

What is the difference between Medical Content Review vs Medical Writer?

AspectMedical Content ReviewMedical Writer
Primary RoleReviewing and validating medical content for accuracy and complianceCreating, drafting, and editing medical content and documents
Required CredentialsMedical background, often with healthcare or clinical experienceMedical or scientific degree, strong writing skills
Work EnvironmentPharmaceutical companies, medical communication agencies, regulatory bodiesPharmaceutical companies, medical publishing, marketing teams
FocusEnsuring content accuracy and regulatory complianceProducing clear, engaging, and scientifically accurate content

Medical Content Review and Medical Writer roles both require a strong medical background, but differ in focus. Reviewers primarily verify content accuracy and compliance, while writers focus on creating and editing medical documents. Both roles are essential in the medical communication industry and often collaborate to produce high-quality medical content.

What are the key skills and qualifications needed to thrive as a Medical Content Reviewer, and why are they important?

To thrive as a Medical Content Reviewer, you need a strong background in life sciences or medicine, excellent research skills, and attention to detail, usually backed by relevant degrees or certifications. Familiarity with medical databases, reference management tools, and content management systems is typically required. Strong analytical thinking, effective communication, and the ability to interpret complex scientific information are crucial soft skills in this role. These competencies ensure the accuracy, clarity, and reliability of medical content, which is vital for maintaining trust and compliance in healthcare communications.
More about Medical Content Review jobs
What cities are hiring for Medical Content Review jobs? Cities with the most Medical Content Review job openings:
What states have the most Medical Content Review jobs? States with the most job openings for Medical Content Review jobs include:
What job categories do people searching Medical Content Review jobs look for? The top searched job categories for Medical Content Review jobs are:
Medical Content Review jobs near you
Infographic showing various Medical Content Review job openings in the United States as of June 2026, with employment types broken down into 77% Full Time, 8% Part Time, 2% Temporary, and 13% Contract. Highlights an 80% In-person, 5% Hybrid, and 15% Remote job distribution, with an average salary of $80,932 per year, or $38.9 per hour.

Manager, Medical Information

Sequel Med Tech

Marlborough, MA

Full-time

Posted yesterday

Be an early applicant

Job description

About Sequel 
Sequel, headquartered in Manchester, New Hampshire, is a company developing the next generation of transformative drug-delivery advancements starting with diabetes. Sequel’s approach is to look at diabetes management holistically to advance systems that make living with diabetes simpler and easier for all. Sequel’s flagship product, the twiist Automated Insulin Delivery (AID) System, launched in July 2025 for people with type 1 diabetes providing them with personalized diabetes management.  
 
Job Overview

The Medical Information Manager serves as a central scientific resource within Medical Affairs, responsible for delivering accurate, balanced, and compliant medical information to internal and external stakeholders. Working closely with the Chief Medical Officer and the broader Medical Affairs team, this role owns the development and maintenance of standard medical response documents and the company’s medical information repository, ensuring healthcare professionals, patients, and internal partners receive timely, evidence-based responses to medical inquiries about Sequel’s products. 

This role also supports the Medical, Legal, and Regulatory (MLR) review of promotional and scientific materials and contributes to Medical Education initiatives, translating scientific evidence into clear, unbranded content for healthcare professional audiences. The Medical Information Manager safeguards scientific and regulatory integrity across all communications while helping Medical Affairs serve as a trusted resource across the organization. 

Job Responsibilities and Essential Duties:

  • Medical inquiries: 

  • Respond to verbal and written medical inquiries from internal and external customers  

  • Preview standard medical response letters and revises or develops new letters as needed. Proactively develop medical response documents. 

  • Stakeholder Collaboration: 

  • Work closely with the Medical Affairs team, including medical directors, scientists, and the Chief Medical Officer, to gather and verify information. 

  • Coordinate with the marketing and public relations teams to align medical communications with broader company messaging. 

  • Proofreading and Quality Control: 

  • Perform meticulous proofreading and editing of all medical content to ensure grammatical accuracy, clarity, and consistency. 

  • Implement quality control measures to ensure all publications meet high standards of excellence. 

  • Promotional and Scientific Materials: 

  • Manage the preparation and submission of medical content to the Medical, Legal, and Regulatory (MLR) and Scientific Material Review process. 

  • Perform medical accuracy review of promotional materials containing medical content 

  • Ensure all content complies with regulatory and company standards before submission. 

  • Track and manage feedback from reviewers and implement necessary revisions. 

  • Medical Inquiries Resource Development and Support 

  • Develop, organize, and maintain the company’s repository of standard medical responses, FAQs, and reference materials. 

  • Ensure all medical inquiry resources are scientifically accurate, compliant, and aligned with regulatory and company standards. 

  • Provide ongoing updates and maintenance of these resources in response to new evidence, product updates, and regulatory guidance. 

  • Support Medical Affairs and cross-functional teams by ensuring timely access to accurate, approved medical content for responding to inquiries. 

  • Regulatory Compliance: 

  • Ensure all communications comply with relevant regulatory requirements and ethical standards. 

  • Stay updated on industry guidelines and best practices for medical and scientific communication. 

  • Medical Education: 

  • Create unbranded presentations for Medical Affairs use 

  • Translate scientific results for use in Medical Education presentations 

  • Development of scientific summaries for distribution to HCPs 

  • Compile & synthesize HCP insights to build scientific and education priorities 

Minimum Requirements (Education and Experience):

  • Education: Advanced degree in medicine, pharmacy, nursing, or life sciences (MD, PharmD, PhD, NP, PA, or equivalent). 

  • Experience: 5+ years of relevant industry experience in medical safety, pharmacovigilance, clinical research, or medical affairs. 

  • Experience in the medical device and/or pharmaceutical industry with exposure to post-market surveillance and safety reporting. 

Required Knowledge, Skills and Abilities:

  • Medical Information & Scientific Communication: Strong writing and editing skills to prepare medical response letters, scientific summaries, and HCP-facing content with accuracy and clarity. 

  • Strong understanding of diabetes management and familiarity with insulin pump therapy preferred. 

  • Medical Information Management: Experience developing and maintaining standard response documents, FAQs, and medical information repositories. 

  • MLR & Compliance Fluency: Familiarity with the Medical, Legal, and Regulatory review process and standards for promotional and scientific materials. 

  • Data Interpretation & Statistical Literacy: Ability to interpret clinical and real-world data—including study endpoints, confidence intervals, and effect sizes—and communicate findings accurately to scientific and lay audiences. 

  • Medical Education Support: Ability to translate scientific evidence into clear, unbranded educational content for HCP audiences. 

  • Collaboration: Proven ability to partner effectively across Medical Affairs, Regulatory, Marketing, and Commercial teams to align messaging and ensure compliance. 

  • Quality & Compliance Focus: Commitment to high standards of accuracy, regulatory compliance, and ethical practice in all deliverables. 

  • Organizational Skills: Ability to manage multiple projects, prioritize effectively, and deliver under tight timelines. 

  • Interpersonal Skills: Strong influencing, facilitation, and presentation abilities; capable of serving as a medical information subject matter expert internally and externally. 

Sequel Med Tech provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. 
 
At Sequel, we believe that when you thrive, we thrive. That’s why our benefits package is designed to support you from day one. You’ll be automatically enrolled in our 401k plan, featuring a 6% company match and 100% immediate vesting. We’re committed to your well-being and understand the unique needs of employees and families living with diabetes, so we offer capped out-of-pocket insulin costs and GLP-1 coverage across all plans. You’ll have access to a variety of Meritain health insurance plans to suit your needs and can also take advantage of Flexible Spending Accounts (FSAs) or Health Savings Account (HSA). Our comprehensive benefits package includes vision and dental coverage, plus voluntary options such as long-term disability, accident, critical illness, hospital indemnity, and even discounts for pet care. In addition, we provide employer-paid short-term disability and life insurance for extra peace of mind.

We know the importance of taking time to rest and recharge. That’s why Sequel offers flexible PTO, generous paid holidays, and Flex Time options to help you balance work and life when you need it most. Our team enjoys a culture built on hard work, fun, and genuine support. At Sequel, you’re not just starting a job, you’re building a rewarding career and a brighter future. Join us, and let’s thrive together!
 
Environmental/Safety/Physical Work Conditions 
Ensures environmental consciousness and safe practices are exhibited in decisions 
Use of computer and telephone equipment and other related office accessories/devices to complete assignments 
May work extended hours during peak business cycles 
Physical requirements such as lifting specific weights 
Some travelling is expectedÂ