ZipRecruiter

Log In

2

Remote Medical Writer Jobs (NOW HIRING)

Pulse Biosciences

Medical Writer

About the Role The Medical Writer develops, writes, and edits high-quality clinical and regulatory documentation required to support the development, registration, and post-market surveillance of ...

Medasource

HEOR Medical Writer

Whippany, NJ · On-site +1

$30 - $40/hr

Medical Writer - Clinical Content & Health Economics and Outcomes Research (HEOR), Clinical Content ... Remote Duration: 6 month contract with the potential for extension, based on performance Targeted ...

ImmunityBio, Inc.

Senior Medical Writer

The Senior Medical Writer will also be responsible for more complex writing assignments and will serve as subject matter expert within the department. The Senior Medical Writer may also be ...

Argenx

Senior Medical Writer

$128K - $176K/yr

For the expansion of our team, argenx is looking for a Senior Medical Writer who will provide medical writing support for developing complex clinical, nonclinical, and safety documents for regulatory ...

4D Molecular Therapeutics

Principal Medical Writer

The Principal Medical Writer will support 4D-150, a gene therapy in late-stage development for retinal vascular diseases, including nAMD and DME, and associated BLA-enabling activities as well as ...

Praxis Precision Medicines, Inc.

Senior Medical Writer

$130K - $150K/yr

The Opportunity This role is responsible for medical writing activities for one or more clinical development programs at Praxis, as directed by the Associate Director, Medical Writing. The individual ...

Syneoshealth

Principal Medical Writer - Publications

OR · Remote

Principal Medical Writer - Publications Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point ...

Olema Oncology

Lead Senior Medical Writer

San Francisco, CA · On-site +1

$160K - $175K/yr

About the Role >>> Lead Senior Medical Writer As the Lead Senior Medical Writer, reporting to the ... Experience working in hybrid/remote environments Attributes: * Teamwork and collaboration; balances ...

Real Chemistry

Senior Medical Writer

The Senior Medical Writer serves as an integral part of the Real Chemistry Medical Communications division in developing scientific content in support of a variety of omnichannel medical ...

Olema Oncology

Lead Senior Medical Writer

Boston, MA · On-site +1

$160K - $175K/yr

About the Role >>> Lead Senior Medical Writer As the Lead Senior Medical Writer, reporting to the ... Experience working in hybrid/remote environments Attributes: * Teamwork and collaboration; balances ...

next page

Showing results 1-20

People also search for

All JobsRemote Medical Writer Jobs

Remote Medical Writer information

See salary details

$14

$38

$57

How much do remote medical writer jobs pay per hour?

As of May 31, 2026, the average hourly pay for remote medical 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 Does a Remote Medical Writer Do?

As a remote medical writer, your duties are to work from home and write documents or articles for medical journals, promotional materials, and reports. In this position, you may collect medical information from clinical studies, examine the protocols used in those studies, and edit documents to ensure the clarity and consistency of the content. Most medical writers specialize in a particular type of content, such as writing research proposals or filling out paperwork for regulatory submissions. Although this is a remote position, companies tend to prefer applicants who are located in the same part of the country to make it easier to coordinate schedules and answer questions as needed.

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

To thrive as a Remote Medical Writer, you need strong scientific knowledge, excellent writing skills, and a relevant degree in life sciences or medicine. Familiarity with referencing software, document management systems, and guidelines like ICMJE or AMA is typically required, along with experience using tools such as EndNote or PubMed. Attention to detail, time management, and the ability to communicate complex information clearly are standout soft skills for this role. These abilities are essential for producing accurate, credible, and timely medical content that meets regulatory and publication standards.

How do Remote Medical Writers typically collaborate with subject matter experts and project teams while working offsite?

Remote Medical Writers often work closely with physicians, researchers, and regulatory professionals through virtual meetings, emails, and collaborative document platforms. Regular communication is essential to clarify scientific content, gather feedback, and ensure accuracy in documentation. Tools like Microsoft Teams, Zoom, and cloud-based editing platforms facilitate real-time collaboration and version control. Building strong working relationships and maintaining proactive communication are key to overcoming the challenges of remote teamwork in this role.

What are remote medical writers?

Remote medical writers are professionals who create scientific documents, such as clinical study reports, regulatory submissions, medical articles, and educational materials, while working from a location outside of a traditional office setting. They typically have expertise in medical science and strong writing skills, enabling them to communicate complex medical information clearly and accurately. Remote medical writers often collaborate with healthcare professionals, researchers, and pharmaceutical companies using digital tools. Their work is crucial for ensuring that medical content is accurate, compliant with regulations, and accessible to its target audience. This role allows for location flexibility and is increasingly in demand within the healthcare and pharmaceutical industries.

What is the difference between Remote Medical Writer vs Medical Communications Specialist?

AspectRemote Medical WriterMedical Communications Specialist
Required CredentialsTypically requires a degree in life sciences, healthcare, or related field; often a medical or scientific writing certificationSimilar credentials; may also require training in medical communication or marketing
Work EnvironmentPrimarily remote, working independently on scientific documentsOften collaborative, working with teams on strategic communication projects
Employer & Industry UsagePharmaceutical, biotech, and healthcare companies; contract agenciesPharmaceutical companies, medical education agencies, and healthcare marketing firms
Common Search & Comparison IntentYesYes

Remote Medical Writers focus on creating scientific documents independently, often remotely, while Medical Communications Specialists typically work in teams to develop broader communication strategies. Both roles require similar scientific backgrounds and are prevalent in healthcare industries, but their daily tasks and collaboration levels differ.

More about Remote Medical Writer jobs
What cities are hiring for Remote Medical Writer jobs? Cities with the most Remote Medical Writer job openings:
What are the most commonly searched types of Medical Writer jobs? The most popular types of Medical Writer jobs are:
What states have the most Remote Medical Writer jobs? States with the most job openings for Remote Medical Writer jobs include:
What job categories do people searching Remote Medical Writer jobs look for? The top searched job categories for Remote Medical Writer jobs are:
Remote Medical Writer jobs near you
Infographic showing various Remote Medical Writer job openings in the United States as of May 2026, with employment types broken down into 82% Full Time, 17% Part Time, and 1% Contract. Highlights an 6% Physical, and 94% Remote job distribution, with an average salary of $80,364 per year, or $38.6 per hour.
Medical Writer

Medical Writer

Pulse Biosciences

Remote

Full-time

Medical, Retirement, PTO

Posted 20 days ago

Job description

Pulse Biosciences (Nasdaq: PLSE): Join the Future of Bioelectric Medicine
Pulse Biosciences is a novel bioelectric medicine company committed to health innovation that has the potential to improve the quality of life for patients. The Company's proprietary CellFX® nsPFA™ (nanosecond Pulsed Field Ablation) technology delivers nanosecond pulses of electrical energy to non-thermally ablate cells while sparing adjacent noncellular tissue.
The Company is actively pursuing the development of its CellFX nsPFA technology for use in the surgical treatment of atrial fibrillation and percutaneously in a select few other markets where it could have a profound positive impact on healthcare for both patients and providers. Visit pulsebiosciences.com to learn more.
Why Join Us?
At Pulse Biosciences, we are driven by purpose and innovation.
  • Our Mission: To build a viable Company that designs, produces, and commercializes nano-pulse technology to improve and extend the lives of patients. To solve the needs of patients, physicians, and healthcare providers with high quality and high reliability products and services, developed in accordance with rigorous scientific, engineering, and clinical standards. We exist to make a positive difference in the lives of patients, physicians, healthcare providers, shareholders and our Pulse Biosciences team members.
  • Our Culture: A community of creative, forward-thinking individuals tackling challenges with ingenuity and collaboration.
  • Our Commitment: Hiring the best and brightest minds to advance our world-class organization.

What You Will Experience:
  • Culture and Purpose - Purposeful and rewarding work collaborating with bright and curious minds brings us together!
  • Innovative Environment - An environment that fosters innovation to take products from concept to human use quickly!
  • Growth Opportunities - Learning culture focusing on professional and personal growth and development that you can only get in a startup-like environment!
  • Comprehensive Benefits - A variety of health insurance plans and supplemental insurance options, and 401k retirement savings plan.
  • Ownership and Rewards - Stock options awards and Employee Stock Purchase Plan (ESPP) to share in our success.
  • Work-Life Balance - Enjoy paid time off, paid holidays, flexible work schedule and wellness program, including onsite gym and mindfulness classes.
  • Diversity & Inclusion - A commitment to providing a respectful work environment to our diverse workforce.

About the Role
The Medical Writer develops, writes, and edits high-quality clinical and regulatory documentation required to support the development, registration, and post-market surveillance of medical devices. This role works closely with Clinical Affairs, Regulatory Affairs, R&D, and Quality Engineering to interpret clinical data and ensure compliance with global standards.
To Make an Impact, You Will:
  • Audit, edit, and maintain clinical and regulatory documents, including Clinical Evaluation Reports (CERs), Clinical Study Protocols and Reports (CSPs/CSRs), Investigator's Brochures (IBs), IFUs, Post-Market Clinical Follow-up (PMCF) plans and reports, and risk management documentation .Ensures compliance to applicable regulations and guidance's (ISO13485, ISO14155, ISO14791,, MDR, and EU and FDA guidance documents) and applicable Pulse Biosciences SOPs.
  • Collaborate with Clinical, Regulatory, Quality, Biostatistics and R&D Engineering to ensure aligned messaging and data interpretation.
  • Conduct literature reviews and synthesize clinical data from multiple sources.
  • Review and edit manuscripts for submission and publication in peer-reviewed journals.
  • Translate complex scientific and clinical information into clear, concise and regulatory-compliance narratives.
  • Support document strategy, timelines and regulatory submissions (e.g. FDA, PMA, CE marking technical documentation).
  • Involved in responses to complex queries such as those issued by notified bodies and stakeholder.
  • Maintain document consistency, version control, and audit readiness.
  • Contribute to SOP development and process improvements.

To Excel, You Will Bring:
  • BS in Life Sciences, Medical Technology, Engineering, related scientific field or relevant experience required.
  • 5+ years of medical writing experience in the medical device or pharmaceutical industry or 7+ years general technical writing.
  • Writing, editing and managing clinical and technical documentation utilized in the development of new products and improvement of existing products.
  • Experience supporting FDA submissions.
  • Excellent writing, editing and communication skills.
  • Strong knowledge of clinical research methodologies and evidence generation for medical device.
  • Strong knowledge of ISO 14155 and EU MDR or FDA regulatory requirements.
  • Proficient knowledge and skill in Microsoft Office Suite applications and document management systems.
  • Ability to interpret and create complex tabular and graphical clinical data presentations.
  • Proficiency in using database tools, such as PubMed, EMBASE, or MEDLINE
  • Excellent scientific writing skills, including an ability to summarize and interpret complicated data effectively, concisely and persuasively.
  • Knowledge of additional languages is an asset.
  • Strong attention to detail.
  • Ability to work conscientiously and with minimal direction, using good judgment, taking initiative to accomplish short and long-range projects, and recommend actions with minimal direction.
  • Ability to work as a team member, manage multiple projects and deadlines and be very flexible to adapt to the ever-changing work priorities and requirements of a dynamic, fast-growing company.
  • Ability to lift 10-15 pounds.

Ready to Shape the Future of Healthcare?
Apply today to join Pulse Biosciences and help us redefine the boundaries of medicine with bioelectric innovation. To learn more about us, visit our website at www.pulsebiosciences.com.
We provide equal employment opportunities (EEO) to all persons regardless of race, age, color, gender, sexual orientation, national origin, physical or mental disability, religion, or any other characteristic protected by federal, state or local law. We will make reasonable accommodations for qualified individuals with disabilities.
PRINCIPALS ONLY; UNSOLICITED CANDIDATE SUBMISSIONS FROM RECRUITERS OR THIRD-PARTY AGENCIES WILL BE CONSIDERED FREE REFERRALS.

Apply