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How much do medical publications manager jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for medical publications 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.

What skills and qualifications are needed to be a medical publications manager?

To thrive as a Medical Publications Manager, you need a solid background in life sciences, experience in scientific writing, and familiarity with publication guidelines such as GPP and ICMJE. Proficiency with reference management software, publication planning tools, and often a relevant certification (e.g., CMPP) is highly valued. Exceptional project management, attention to detail, and strong interpersonal skills set outstanding candidates apart. These abilities are crucial for ensuring timely, compliant, and impactful dissemination of scientific information to the medical community.

How does a medical publications manager collaborate with cross-functional teams during the publication development process?

A Medical Publications Manager plays a central role in coordinating with various cross-functional teams such as medical writers, clinical researchers, regulatory affairs, and marketing to ensure accuracy and compliance in publication content. They facilitate regular meetings to align on timelines, data interpretation, and messaging, while also managing external agencies and key opinion leaders for manuscript development and review. Effective collaboration helps streamline the approval process and ensures that all publications adhere to industry standards and company policies.

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

AspectMedical Publications ManagerMedical Writer
CredentialsTypically requires a degree in life sciences, healthcare, or related field; often advanced degrees or certifications in medical writing or publication managementUsually holds a degree in life sciences, healthcare, or communications; certifications like AMWA or EMWA are common
Work EnvironmentManages publication projects, coordinates with authors, and oversees publication strategies within pharmaceutical or healthcare companiesPrepares, writes, and edits scientific documents, including manuscripts, regulatory documents, and promotional materials
Employer & Industry UsageUsed in pharmaceutical, biotech, and healthcare industries for publication planning and managementCommonly employed in medical communication agencies, pharmaceutical companies, and research institutions for content creation

The Medical Publications Manager focuses on overseeing publication strategies and managing teams, while the Medical Writer is primarily responsible for creating and editing scientific content. Both roles require relevant scientific knowledge and communication skills, but their core responsibilities differ significantly.

What does a medical publications manager do?

A Medical Publications Manager oversees the development, review, and dissemination of scientific and medical information produced by a pharmaceutical or healthcare company. Their responsibilities include managing the creation of manuscripts, abstracts, posters, and presentations for medical conferences and journals. They collaborate with medical writers, researchers, and key opinion leaders to ensure accuracy, compliance with regulations, and alignment with strategic objectives. Additionally, they help ensure that publication plans support the communication of clinical trial results and other research findings to the medical community.
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Medical Publications Manager jobs near you
Infographic showing various Medical Publications Manager job openings in the United States as of August 2026, with employment types broken down into 75% Full Time, and 25% Contract. Highlights an 50% In-person, and 50% Remote job distribution, with an average salary of $92,054 per year, or $44.3 per hour.

Scientific Director - Publications (Oncology, CAR T)

The Lockwood Group, LLC

Remote

Full-time

Re-posted 4 days ago

Job description

This position can be based remotely (working from home) or at our headquarters in Stamford, CT.
About Lockwood: Lockwood collaborates with clients in the pharmaceutical, biotech, and medical device industries to identify effective, holistic, science-based strategies to address their objectives through medical communications. Our clients count on us to challenge their assumptions and help them creatively navigate around obstacles. From strategy through execution, we focus on accuracy, transparency, and scientific value to create programs that are evidence-based, clinically relevant, and contribute to the development of our clients' brands. Over a third of our staff hold advanced scientific or medical degrees, and most work from where they live. Because our flexible structure provides better work-life balance, we attract the best talent, facilitate their best work, and as a result, are more responsive to our clients, wherever and whenever they do business.
Summary: In this role, the Scientific Director is responsible for the planning, development, and oversight of scientific content for an assigned account or accounts across various therapeutic areas addressing different target audiences.
Responsibilities: Responsibilities include working with the Group Scientific Director to provide clients with strategic medical communication recommendations that support the achievement of brand goals, independently leading execution of content development activities, supervising Associate Scientific Directors, and liaising with other in-house or freelance staff to manage writing and other content-related tasks such as conducting background research, data-checking, and reference annotation.
Education: An advanced degree in science (ie. PhD, PharmD, or MD) is required. CMPP preferred.
Professional Skills and Requirements:
  • Candidates must have 5 or more years of relevant job experience with medical publications, including manuscripts, posters, abstracts, podium presentations, scientific platforms, and publication extenders.
  • This role requires demonstrated organizational, analytical, and interpersonal communication skills, as well as the ability to analyze and interpret scientific data, multitask, work independently, and manage projects within tight deadlines.
  • Experience with established professional medical editorial processes (ie. AMA style) and ethical guideline working knowledge (ie. ICMJE, GPP2022) is also required.
  • Experience with Oncology required and CAR T experience is a plus.

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