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Online Medical Writing Jobs (NOW HIRING)

Agomab

Senior Director, Medical Writing

Cambridge, MA · On-site

Senior Director, Medical Writing Department: Regulatory Affairs Employment Type: Permanent - Full Time Location: Agomab US Reporting To: Senior VP/Head of Regulatory Affairs Description This is a ...

Travere

Senior Manager, Medical Writing

San Diego, CA · On-site +1

Department: 107050 Medical Writing Location: San Diego, USA- Remote Be a part of a global team that ... online application, interview or hiring process only. Travere HR will not reply to emails sent to ...

Vaxcyte

Director, Clinical Medical Writing

San Carlos, CA · On-site +1

$221K - $258K/yr

Vaxcyte is seeking a Director, Clinical Medical Writing to drive and shape the medical writing processes, procedures, strategies, and document generation and maintenance. This position will lead ...

Alnylam Pharmaceuticals

Senior Manager, Medical Writing

$146K - $197K/yr

The Senior Manager, Medical Writing will collaborate with project teams on the development of clinical documents in accordance with all applicable regulations, Good Clinical Practices, and Standard ...

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Online Medical Writing information

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How much do online medical writing jobs pay per hour?

As of Aug 3, 2026, the average hourly pay for online medical writing in the United States is $46.27, according to ZipRecruiter salary data. Most workers in this role earn between $33.65 and $56.01 per hour, depending on experience, location, and employer.

What is the difference between Online Medical Writing vs Medical Content Writing?

AspectOnline Medical WritingMedical Content Writing
CredentialsTypically requires a healthcare or scientific background, often with a degree in medicine, pharmacy, or life sciencesOften requires a background in healthcare, communications, or journalism, but less specialized
Work EnvironmentRemote or freelance, working with pharmaceutical companies, healthcare providers, or publishersRemote or freelance, creating content for health websites, marketing, or educational platforms
Industry UsageCommonly used in pharmaceutical, biotech, and clinical research industriesUsed across healthcare marketing, health blogs, and patient education platforms

Online Medical Writing focuses on creating scientifically accurate, regulatory-compliant content for healthcare professionals and industry stakeholders. Medical Content Writing is broader, often aimed at general audiences, including patients and consumers, with a focus on engaging and accessible health information.

What types of projects do online medical writers typically work on, and how do they collaborate with healthcare professionals?

Online medical writers are often involved in creating a range of content, such as patient education materials, regulatory documents, clinical study reports, and digital health articles. They usually collaborate closely with subject matter experts, clinicians, and regulatory teams to ensure content accuracy and compliance with industry standards. Effective communication and the ability to translate complex scientific data into clear, accessible language are essential. Team meetings and regular feedback loops are common, providing opportunities to learn from experts and refine writing based on evolving project needs.

What are the key skills and qualifications needed to thrive as an Online Medical Writer, and why are they important?

To thrive as an Online Medical Writer, you need a strong background in life sciences or medicine, excellent written communication skills, and often a relevant degree such as a BSc or MSc. Familiarity with referencing software (like EndNote), content management systems, and style guides such as AMA or ICMJE is typically required. Attention to detail, the ability to convey complex information clearly, and strong time management are crucial soft skills. These attributes ensure the production of accurate, credible, and audience-appropriate medical content for digital platforms.

What is online medical writing?

Online medical writing involves creating, editing, and reviewing scientific documents and content related to medicine and healthcare, specifically for digital platforms. This can include writing articles, regulatory documents, educational materials, and promotional content for websites, blogs, online journals, and social media. Medical writers typically need a strong background in life sciences and the ability to communicate complex information clearly to different audiences, such as healthcare professionals or the general public. The role often requires attention to detail, adherence to ethical standards, and up-to-date knowledge of medical guidelines and digital publishing practices.
More about Online Medical Writing jobs
What cities are hiring for Online Medical Writing jobs? Cities with the most Online Medical Writing job openings:
What are the most commonly searched types of Medical Writing jobs? The most popular types of Medical Writing jobs are:
What states have the most Online Medical Writing jobs? States with the most job openings for Online Medical Writing jobs include:
What job categories do people searching Online Medical Writing jobs look for? The top searched job categories for Online Medical Writing jobs are:
Online Medical Writing jobs near you
Infographic showing various Online Medical Writing job openings in the United States as of July 2026, with employment types broken down into 79% Full Time, and 21% Contract. Highlights an 74% In-person, 5% Hybrid, and 21% Remote job distribution, with an average salary of $96,235 per year, or $46.3 per hour.

Sr. Manager, Medical Writing

Medical Affairs

Somerset, NJ • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 5 days ago

Job description

Terumo Medical Corporation (TMC) develops, manufactures, and markets a complete, solutions-based portfolio of high-quality medical devices used in a broad range of applications for numerous areas of the healthcare industry. TMC places a premium on providing customers with world-class products, training and education programs that drive clear economic value, better clinical outcomes and improved quality of life for patients. TMC is part of Tokyo-based Terumo Corporation; one of the world’s leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide and operations in more than 160 nations. Terumo Medical Corporation is comprised of two strategic business divisions: Terumo Interventional Systems and Terumo Medical Products.

We believe that the future is bright for everyone at Terumo. We work with the future in mind to generate lasting change, create a bigger impact and produce greater outcomes for today, and for decades to come.

At Terumo we believe in the power of personal growth and will encourage you to get in the driver's seat - progressing in the direction you want to go by deepening your skills throughout your career. We want you to be bold, think outside the box, experiment, innovate and deliver what's next for quality healthcare. You will be part of a collaborative, respectful and resilient team of associates and leaders around the world, working together as partners to achieve more than you thought possible, providing real-world, impactful solutions for patients.

Join us and help shape wherever we go next!

Advancing healthcare with heart

Job Summary

Sr. Manager Medical Writing, manages and oversees the work of medical writing teams to support clinical and regulatory submissions (e.g., clinical evaluation reports, clinical study reports,) and product development. This role partners with Engineering and R&D, Clinical Affairs, Professional & Clinical Education, Regulatory Affairs, Quality Systems, Marketing, Sales as well as external stakeholders, to include FDA, NB, PMDA, KOL, HCP, IRB and publishers. The role reports directly to the Senior Medical Director, Scientific Data & Communications.

Job Details/Responsibilities
  • Lead, mentor, and develop a team of medical writers responsible for clinical evaluation, scientific communication, and regulatory documentation. Oversee workload allocation, project prioritization, and timely delivery of high‑quality documents; and lead  talent development in alignment with growth strategies of the department. 40% of role.
  • Provide technical guidance, writing expertise, and scientific oversight to ensure consistency, accuracy, and compliance with applicable regulations and internal standards. Develop and maintain SOPs, work instructions, and best practices related to medical writing. Serve as subject‑matter expert in medical writing standards, expectations of regulatory bodies, and scientific communication. 20% of role. 
  • Review and approve the team outputs including regulatory documents / scientific communication / clinical research related documents. 20% of role. 
  • Assure Quality Oversight & Regulatory Compliance. Oversee literature review methodologies, literature database management practices, and interpretation of scientific evidence. 10% of role.
  • Build and manage internal partnerships with PACE, Clinical Operations, Regulatory Affairs, Quality System and Marketing R&D and Engineering. 10% of role. 
Working Conditions/Physical Requirements
  • This position requires up to 10% of travel
  • Manage a team of 3 direct reports 
Knowledge, Skills and Abilities (KSA)
  • Strong leadership in project and team management, including coaching and performance oversight.
  • Excellent organizational and time management skills
  • Expertise in medical writing processes, regulatory requirements (FDA, EU MDR), with GCP, and ICH guidelines
  • Ability to adapt to changing priorities
  • Knowledge of biomedical statistics, clinical literature review
  • Highly proficient in using Microsoft Office applications (Word, Excel, PowerPoint) and EndNote
  • Expertise in conducting focused literature searches on PubMed, Embase, MedLine or other similar medical literature databases
  • Knowledge and understanding of PICO methodology
  • Ability to function in a self-directed manner with a high degree of independence
  • Strong verbal, written, and interpersonal communication skills
  • Ability to persuasively influence external medical professionals
  • Effective analytical and problem-solving skills
  • Excellent interpersonal and effective leadership, verbal and written communication skills and effectively work across departments with diverse needs
Qualifications/ Background Experiences
  • Advance Degree ((Ph.D., MD, Sc.D, MA/MS or MPH) in a medical/biomedical/scientific discipline with a minimum of 5 years of experience in medical writing of regulatory documentation (clinical research documentation is optional) OR Bachelor’s Degree, preferably in life sciences with 10 years  of relevant work experience; OR equivalent combination of education, training and relevant experience.
  • Demonstrated relevant track record in people management how many years?
  • Experience in medical or scientific writing and creating content for scientific presentations
  • Demonstrated experience in the development of regulatory/clinical submissions, preferably as a medical writer for pharmaceutical, CRO, or medical device clients, a strong plus.
  • Experience with Class III devices and CER development under MDR preferred

It is Terumo’s policy to provide equal employment opportunity to all its employees and applicants for employment regardless of their race, creed, color, national origin, age, ancestry, nationality, marital or domestic partnership or civil union status, sex, pregnancy, gender identity or expression, disability status, liability for military service, protected veteran status, sexual orientation, atypical cellular or blood trait, genetic information (including the refusal to submit to genetic testing), or any other category protected by law. As a Company, we value diversity of background and opinion, and prohibit discrimination or harassment on the basis of any legally protected class in the areas of hiring, recruitment, promotion, transfer, demotion, training, compensation, pay, fringe benefits, layoff, termination or any other terms and conditions of employment.

Final compensation packages may be higher or lower than what is listed, and will ultimately depend on factors including relevant experience, internal equity, skillset, knowledge, geography, education, business needs and market demand. We provide competitive and comprehensive benefit options which include: annual bonus, paid vacation, paid holidays, health, dental and vision benefits, 401(k), with matching contributions, tax advantage savings accounts, legal plan, voluntary life and AD&D insurance, voluntary long-term disability, short term disability, critical illness and accident insurance, parental leave, personal leave, tuition reimbursement, travel assistance, and an employee assistance program. The salary range for this role is $150,000 - $198,000 based on experience plus a 20% target bonus. 

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