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Medical Communication Manager Jobs (NOW HIRING)

Real Chemistry

Senior Medical Writer

As a global agency, we provide a full suite of services across healthcare communications and ... Support project management within the cross-functional team by effectively communicating and ...

Taiho Oncology

$140K - $165K/yr

The Manager, Medical Communications, is a key member of the medical communications team ... Excellent written and verbal communication skills. Strong attention to detail and ability to ...

VML

Medical Editor - Freelance

New York, NY · Hybrid

$55/hr

As a Medical Editor - Freelance you will manage all editorial requirements of assigned projects and ... Copy edit and proofread various types of medical communication materials for syntax/grammar ...

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How much do medical communication manager jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for medical communication manager in the United States is $44.26, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $57.69 per hour, depending on experience, location, and employer.

How does a Medical Communication Manager typically collaborate with cross-functional teams within a pharmaceutical company?

Medical Communication Managers work closely with medical affairs, regulatory, marketing, and clinical development teams to ensure scientific accuracy and consistency in all external and internal communications. They often facilitate the review and approval process for medical content, coordinate input from subject matter experts, and provide guidance on compliance with industry regulations. Effective collaboration and clear communication are essential, as these managers bridge scientific knowledge and business objectives to support product strategy and educational initiatives.

What is a Medical Communication Manager?

A Medical Communication Manager is a professional responsible for developing, managing, and disseminating scientific and medical information to healthcare professionals, regulatory agencies, and sometimes the public. They ensure that all communications are accurate, clear, and comply with regulatory standards. Their role often involves collaborating with medical writers, regulatory affairs teams, and marketing departments to create educational materials, publications, and presentations. Medical Communication Managers play a crucial role in supporting the safe and effective use of medical products by providing up-to-date and evidence-based information.

What is the difference between Medical Communication Manager vs Medical Writer?

AspectMedical Communication ManagerMedical Writer
CredentialsTypically requires advanced degrees (MD, PhD, PharmD) and experience in medical communicationsUsually holds a degree in life sciences, communications, or related fields; certifications like AMWA or EMWA are common
Work EnvironmentManages teams, coordinates projects, liaises with clients and stakeholders in pharmaceutical or healthcare companiesFocuses on creating scientific content, often working independently or in small teams, within publishing or agency settings
Employer & Industry UsageUsed in pharmaceutical, biotech, and healthcare industries for strategic communicationCommonly employed in medical publishing, regulatory writing, and pharmaceutical marketing

The Medical Communication Manager oversees communication strategies, manages teams, and liaises with clients, requiring leadership skills and industry experience. In contrast, Medical Writers primarily focus on producing scientific content, requiring strong writing skills and scientific knowledge. Both roles are essential in medical communications but differ in scope and responsibilities.

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

To thrive as a Medical Communication Manager, you need a strong background in life sciences or healthcare, excellent writing and editing skills, and often an advanced degree such as a PharmD, PhD, or MD. Familiarity with regulatory guidelines, publication management systems, and reference management tools is typically required. Exceptional project management, attention to detail, and the ability to communicate complex scientific concepts to diverse audiences are vital soft skills. These competencies ensure accurate, compliant, and impactful communication of medical information to both internal and external stakeholders.
What states have the most Medical Communication Manager jobs? States with the most job openings for Medical Communication Manager jobs include:
What job categories do people searching Medical Communication Manager jobs look for? The top searched job categories for Medical Communication Manager jobs are:
Medical Communication Manager jobs near you
Infographic showing various Medical Communication Manager job openings in the United States as of June 2026, with employment types broken down into 86% Full Time, and 14% Part Time. Highlights an 93% In-person, and 7% Hybrid job distribution, with an average salary of $92,054 per year, or $44.3 per hour.

Manager Medical Communication

Sequel Med Tech

Manchester, NH • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 11 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 Manager of Medical Communications willbe responsible fordevelopingandmaintaininghighquality scientific and medical materials that support healthcare provider (HCP) engagement, product understanding, and safe and effective use of Sequel products. 

The Manager willown the creation and maintenance ofstandard response letters, HCP-facing scientific materials, and scientific slide decks. They willmanage Sequel's publication roadmap,  including planning, prioritization, and stakeholder alignment, andserve as a primary author/medical writerfor abstracts, posters, manuscripts, and congress content. This individual will collaborate closely with Medical, Regulatory, Legal, and external partners to ensure accuracy, compliance, and consistency across all scientific communications. 

This role is ideal for a PharmD or advanced scientific professional with strong writing ability and experience in medical information, publications, and scientific communication.

Job Responsibilities and Essential Duties:

Medical Information & Standard Response Development 

  • Develop, update, andmaintainstandard medical response letters for internal and external inquiries, ensuring scientific accuracy, clarity, and regulatory compliance. 

  • Create and manage a repository of medical responses, FAQs, data summaries, and reference materials forcross functionaluse. 

  • Review and refine medical inquiry responses to ensure alignment with company messaging and relevant regulations. 

  • Develops responses to unsolicited HCP requests for off-label scientific information consistent with FDA scientific exchange guidance 

Scientific & HCP Material Development 

  • Develop andmaintainHCPfacing materials including clinical slide decks, scientific summaries, data sheets, and educationmaterials. 

  • Translate complex clinical and scientific information into clear, engaging, andaccuratecontent suitable for diverse audiences. 

Publications & Evidence Dissemination 

  • Manage Sequel's publication roadmap, including planning, prioritization, timelines, internal alignment, and stakeholder communication. 

  • Author and co-author scientific publications,  abstracts, posters, manuscripts, and congress materials,  drafting, revising, and finalizing content with internal SMEs and external collaborators. 

  • Coordinate with internal SMEs and external partners (e.g., investigators, agencies, KOLs) on authorship, ICMJE compliance, and conflict-of-interest disclosures. 

  • Track progress, manage deadlines, and facilitate submissions for abstracts, posters, manuscripts, and congress materials. 

CrossFunctionalCollaboration 

  • Partnerwith Medical Affairs leadership, Clinical, Regulatory, Quality, Marketing, and external collaborators to ensure alignment and scientific rigor across all communications. 

  • Support review cycles for promotional and scientific materials, ensuring accuracy and compliance prior to MLR submission 

  • Serve as a scientific resource for internal teams, helping drive consistency in messaging and evidence use 

  • Serve as the primary Medical Affairs subject matter expert and point of contact for the medical communications technology platform 

Presentation & Engagement Support 

  • Develop and deliver internal and external PowerPoint presentations, including data overviews, training decks, and congress content. 

  • Provide scientific writing and editorial support for a range of internal and external communication needs. 

Quality, Compliance & Documentation 

  • Ensure all content adheres to regulatory standards, company policies, and quality management requirements 

  • Maintainaccuratedocumentation of materials, versioning, references, and approval history. 

Minimum Requirements (Education and Experience):

  • Education: PharmD strongly preferred; alternatively,PhD, MD, MS, or equivalent advanced scientific degree withdemonstratedexpertisein medical communications within healthcare technology. 

  • Experience: 3+ years of experience in medical communications or medical information within a medical device, digital health, orMedTechcompany, ideally supporting FDAregulated products 

  • Experience working in diabetes, metabolic disease, endocrinology, or automated insulin delivery (AID) systems;either through prior roles, fellowship training, publications, or direct industry exposure.

Required Knowledge, Skills and Abilities:

  • Proven ability tointerpret clinical data relevant to diabetes care, including CGM, pump therapy, AID algorithms, andrealworldevidence, and translate this into scientificallyaccuratematerials. 

  • Comfort with TIR/TBR/GMI metrics, paired analyses, and basic interpretation of propensity-matched RWE 

  • Demonstrated experience developingHCPfacingscientific resources, standard response letters, or medical information content in an environment with structuredMedical Materials review processes(Medical/Legal/Regulatory). 

  • Proficiencyinmedical device labeling rules, scientific exchange standards, andappropriate managementof onand off-label communication for FDAregulations. 

  • Strong capability increating scientific slide decks and datadriven presentationsfor internal and external audiences. 

  • Demonstrated track record of personally authoring peer-reviewed publications(first or contributing author on abstracts, posters, and manuscripts)in addition to managing publication plansincluding congress submissions and scientific narratives 

  • Ability to work cross-functionally with clinicians, engineers, regulatory affairs, quality, marketing, and external collaborators typical of medtech organizations 

  • Exceptional written communication skills with meticulous attention to scientific accuracy and regulatory compliance. 

  • Comfortable working in arapiditeration, innovationfocusedmedtechenvironmentwhere systems evolve quickly and evidence generation isongoing. 

$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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