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Medical Information Jobs (NOW HIRING)

The Medical Information Specialist III is a frontline specialist responsible for engaging customers, /healthcare professionals, in a robust clinical dialogue. The specialist serves as a primary ...

$175K - $206K/yr

The Sr. Manager, Medical Information & Operations contributes tactical and scientific inputs for the development and delivery of high-quality medical information for assigned Taiho Oncology products.

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The Medical Information Specialist III is a frontline specialist responsible for engaging customers, /healthcare professionals, in a robust clinical dialogue. The specialist serves as a primary ...

OR · On-site

The Medical Information Specialist III is a frontline specialist responsible for engaging customers, /healthcare professionals, in a robust clinical dialogue. The specialist serves as a primary ...

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Medical Information information

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How much do medical information jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for medical information in the United States is $39.04, according to ZipRecruiter salary data. Most workers in this role earn between $32.69 and $45.67 per hour, depending on experience, location, and employer.

What is Medical Information?

Medical Information refers to the function within pharmaceutical, biotechnology, or medical device companies that provides accurate, unbiased, and up-to-date information about products to healthcare professionals, patients, and other stakeholders. Professionals in Medical Information respond to inquiries about drug uses, side effects, dosing, and safety, ensuring that information shared is scientifically validated and compliant with regulations. This role supports safe and effective use of therapies by ensuring access to reliable data and facilitating communication between the company and the medical community.

How does a Medical Information professional typically interact with healthcare providers and internal teams?

Medical Information professionals serve as a vital bridge between pharmaceutical companies and healthcare providers, responding to medical inquiries about products and providing accurate, scientifically balanced information. They frequently collaborate with colleagues in regulatory affairs, pharmacovigilance, and medical affairs to ensure responses comply with industry standards and regulations. Regular communication with sales and marketing teams also helps them stay updated on product developments and align messaging. Building strong relationships and maintaining up-to-date knowledge are critical for success in this collaborative, fast-paced environment.

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

To thrive as a Medical Information Specialist, you need a solid background in life sciences or pharmacy, strong analytical skills, and attention to detail, often supported by a relevant degree. Familiarity with medical databases, literature search tools, pharmacovigilance systems, and regulatory compliance standards is essential. Excellent written and verbal communication, customer service orientation, and problem-solving abilities help you respond accurately to inquiries from healthcare professionals and patients. These skills ensure the delivery of reliable, compliant medical information, which supports patient safety and maintains organizational credibility.
What cities are hiring for Medical Information jobs? Cities with the most Medical Information job openings:
What are the most commonly searched types of Medical Information jobs? The most popular types of Medical Information jobs are:
What states have the most Medical Information jobs? States with the most job openings for Medical Information jobs include:
Infographic showing various Medical Information job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 79% Full Time, 18% Part Time, and 2% Contract. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $81,205 per year, or $39 per hour.

Manager, Medical Information

Sequel Med Tech

Marlborough, MA

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 5 days ago


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. 

$130,000 - $140,000 a year
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 expected 
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