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Health Writer Jobs (NOW HIRING)

BTAS

Writer

El Segundo, CA

$112K - $200K/yr

Writer LOCATION: El Segundo, CA REQUIRED SECURITY CLEARANCE: Active TS with SCI eligibility ... A comprehensive benefits program, including paid time off, federal holidays, health coverage, 401K ...

Heart of Ohio Family Health

Grant Writer

Columbus, OH · On-site

$64K - $91K/yr

Summary: The Grant Writer position is responsible for identification, writing, management, and ... Heart of Ohio Family Health operates in multiple locations in Columbus, OH area. Facilities are a ...

BioPoint Inc

Narrative Writer

Wakefield, MA · Remote

... drug safety, health economics and outcomes research, regulatory affairs, quality assurance ... My Client is in need of a Clinical Narrative Writer. The position is a 3 month, 40 hour a week ...

Oran Inc

Technical Writer

Herndon, VA

Position Title Technical Writer Overview We are seeking a Technical Writer to develop and maintain technical, scientific, and regulatory documentation supporting federal or healthcare programs. The ...

Harvard University

Scientific Writer

Cambridge, MA · On-site

JOB RESPONSIBILITIES The Harvard Global Health Institute (HGHI) serves as the connective tissue for ... HGHI seeks a Scientific Writer to support the institute's scholarly and research mission. Reporting ...

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Health Writer information

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$14

$38

$57

How much do health writer jobs pay per hour?

As of Jul 9, 2026, the average hourly pay for health writer in the United States is $38.64, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $48.80 per hour, depending on experience, location, and employer.

What is the difference between Health Writer vs Medical Writer?

AspectHealth WriterMedical Writer
CredentialsTypically requires a background in health, journalism, or communications; certifications are optionalOften requires a healthcare or scientific degree; certifications like ACR or AMWA are common
Work EnvironmentFreelance, media outlets, health blogs, or corporate content teamsPharmaceutical companies, medical device firms, regulatory agencies, or clinical research organizations
Industry UsageUsed in media, health blogs, and consumer-focused contentUsed in clinical, regulatory, and scientific documentation

Health Writers focus on creating accessible health content for the general public, often working in media or freelance settings. Medical Writers typically produce technical, regulatory, or scientific documents for healthcare professionals or organizations. While both roles require health knowledge, Medical Writers usually have specialized scientific or medical credentials and work in more regulated environments.

What are the key skills and qualifications needed to thrive as a Health Writer, and why are they important?

To thrive as a Health Writer, you need excellent research skills, strong written communication abilities, and a background in health, science, or journalism, often supported by a relevant degree or experience. Familiarity with medical databases, citation tools, and content management systems is typically required. Attention to detail, critical thinking, and the ability to translate complex information for diverse audiences are standout soft skills in this role. These skills and qualities ensure that health information is accurate, accessible, and engaging, supporting public understanding and trust.

What does a health writer do?

A health writer creates content related to health, medicine, and wellness for various audiences, including articles, blog posts, and reports. They research medical topics, interpret scientific data, and communicate complex information clearly, often using writing tools like CMS platforms and adhering to industry guidelines.

How to become a health writer?

To become a health writer, develop strong writing skills and a solid understanding of medical and health topics through education or self-study. Gaining experience by creating a portfolio of health-related articles and staying updated on industry trends can improve job prospects; familiarity with research tools and medical terminology is also beneficial.

How can I get into medical writing with no experience?

Health writers can enter medical writing by gaining foundational knowledge through online courses or certifications in medical or scientific writing. Building a portfolio with sample articles, volunteering, or creating content on health topics can demonstrate skills to employers, even without prior professional experience.

How does a Health Writer typically collaborate with medical professionals and editors during the content creation process?

Health Writers often work closely with subject matter experts, such as doctors and researchers, to ensure the accuracy and credibility of their content. They may conduct interviews, review source materials, and seek clarifications to translate complex medical information into reader-friendly language. Collaboration with editors is also common, as they provide feedback on clarity, tone, and adherence to style guidelines. This teamwork ensures that the final content is both medically accurate and engaging for the target audience.

Do medical writers get paid well?

Health writers, including medical writers, often earn competitive salaries that vary based on experience, education, and specialization. According to industry data, entry-level medical writers typically start around $60,000 annually, with experienced professionals earning over $100,000, especially those with advanced degrees or certifications. The role often requires strong scientific knowledge and writing skills, which can influence compensation levels.

What is a Health Writer?

A Health Writer is a professional who creates clear, accurate, and engaging content related to health, medicine, wellness, and healthcare topics. They translate complex medical information into language that is easy for the general public or specific audiences to understand. Health Writers may work for hospitals, health organizations, media outlets, or as freelancers, and often collaborate with medical experts to ensure accuracy and credibility. Their work can include articles, patient education materials, web content, and more.
More about Health Writer jobs
What cities are hiring for Health Writer jobs? Cities with the most Health Writer job openings:
What are the most commonly searched types of Health Writer jobs? The most popular types of Health Writer jobs are:
What states have the most Health Writer jobs? States with the most job openings for Health Writer jobs include:
Health Writer jobs near you
Infographic showing various Health Writer job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 76% Full Time, 18% Part Time, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $80,364 per year, or $38.6 per hour.
Principal Medical Writer, Cardio/Metabolic Health

Principal Medical Writer, Cardio/Metabolic Health

ProPharma Group

Western Springs, IL • On-site

Full-time

Posted 5 days ago

Job description

For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs.
Essential Functions:
  • Ensures appropriate communication on project- and program-related matters with medical writing leadership, internal functional area heads, and internal resources/consultants as applicable.

  • Manages clinical program documents for assigned clients, such as protocols, protocol amendments, IBs, ICFs, patient narratives, study reports, as well as more complex regulatory documents (e.g., PBRER, IND, NDA, BLA, MAA, eCTD submissionlevel documents) as assigned.

  • Leads cross-functional coordination of resources (e.g., internal resources/consultants) to manage medical writing and QC deliverables as assigned.

  • Independently authors (writes/edits) high-quality medical writing deliverables (i.e., clinical, safety, regulatory, device, diagnostics, or disclosures documents) across all phases of clinical research and in various therapeutic areas including but not limited to: protocols, protocol amendments, study reports, patient narratives, IBs, ICFs, CEPs/CERs, DSURs, and plain language summaries, as well as more complex documents (e.g., PBRER, IND, NDA, BLA, MAA, eCTD submission level documents).

  • Supervises, trains, and mentors less experienced medical writers, as necessary.

  • Adheres to established regulatory standards/guidelines including but not limited to: ICH E3 or E6(R2), EU MDR/IVDR, Company standard operating procedures, client standards, and Company- and/or client-approved templates.

  • Strives to complete medical writing deliverables on time and within budget.

  • Independently manages client expectations and interacts and communicates directly with clients, leads team meetings (e.g., project kickoff, comment review), and manages the deliverable timelines.

  • Interacts and collaborates with subject matter experts in clinical operations, data management, biostatistics, regulatory affairs, etc., as needed, to produce medical writing deliverables.

  • Coordinates QC reviews of documents and maintains audit trails of changes as applicable.

  • Reviews statistical analysis plans and table/figure/listing shells (as applicable) for appropriate content, grammar, format, and consistency.

  • If requested by supervisor, performs QC review (e.g., reviews in-text tables against statistical output).

  • Performs peer review of documents written by other medical writers, as required.

  • Assists with project-related administrative tasks (e.g., creates and maintains timelines, updates deliverable trackers, hosts internal/client meetings).

  • Maintains familiarity with current industry practices, regulatory requirements, and guidelines related to medical writing.

  • Understands budget specifications for assigned deliverables, works within the budgeted hours, and communicates out-of-scope tasks to medical writing leadership.

  • Supports multiple medical writing deliverables/projects simultaneously and manages own workload with minimal intervention from management team.

  • Brings issues and potential concerns to line manager/client oversight manager's attention and proposes possible solutions for consideration by management team.

  • Participates in and leads departmental initiatives (e.g., process improvement, lunch and learns, etc.).

  • Other duties as assigned.

Necessary Skills and Abilities:
  • Advanced knowledge of clinical research principles and demonstrated ability to interpret and present clinical data and other complex information.

  • Advanced understanding of FDA (and other regulatory bodies as relevant to their role) and applicable regulations and guidelines.

  • Advanced understanding of regulatory submission requirements and processes.

  • Computer technology proficiency and expert word processing skills in MS Word, including required proficiency with tables, graphs, and figures.

  • Exceptional project management skills and strong communication skills with a high attention to detail and quality.

  • English language proficiency and familiarity with American Medical Association (AMA) style.

  • Strong experience in relationship building and strategic collaboration on key business accounts.

  • Thinks proactively, takes initiative, and willingly takes on new challenges.

  • Ability to identify areas of concern or inefficiency and propose solutions for consideration by the management team to improve overall efficiency and quality of deliverables.

  • Works independently with exceptional time-management skills and contacts management team proactively when additional support and resources are needed.

  • Works effectively in a collaborative team environment.

  • Demonstrates a growth mindset and positive outlook in all work activities.

Educational Requirements:
  • Bachelor's degree or higher, preferably in medical or scientific discipline.

Experience Requirements:
  • Minimum of 7 years of experience in writing clinical and/or regulatory documents for drugs, biologics, and/or medical devices/diagnostics for a contract research organization, pharmaceutical company, or biotechnology company.

  • Other professional and/or educational experience may contribute toward this minimum requirement, as determined on a casebycase basis.

We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.
Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office.
***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***

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