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Remote Medical Writing Consultant Jobs (NOW HIRING)

CareHarmony

Remote - Medical Receptionist

$14.50/hr

CareHarmony has an immediate opening for a Remote Medical Receptionist with a solid phone presence ... Excellent written and verbal communication skills * Excellent interpersonal and customer service ...

Olema Oncology

Lead Senior Medical Writer

Boston, MA · On-site +1

$160K - $175K/yr

Preparing and editing a wide range of scientific and medical writing deliverables, including but ... Experience working in hybrid/remote environments Attributes: * Teamwork and collaboration; balances ...

Olema Oncology

Lead Senior Medical Writer

San Francisco, CA · On-site +1

$160K - $175K/yr

Preparing and editing a wide range of scientific and medical writing deliverables, including but ... Experience working in hybrid/remote environments Attributes: * Teamwork and collaboration; balances ...

Sygnetics, Inc

Remote Medical Coder II

Louisville, KY · Remote

$38.09/hr

Remote Medical Coder III US Citizenship required. We are currently assembling a team of skilled ... consultations, and concurrent services, and inpatient surgical and anesthesia procedures; and ...

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Remote Medical Writing Consultant information

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$31K

$148.2K

$399K

How much do remote medical writing consultant jobs pay per year?

As of Jun 16, 2026, the average yearly pay for remote medical writing consultant in the United States is $148,159.00, according to ZipRecruiter salary data. Most workers in this role earn between $97,500.00 and $181,500.00 per year, depending on experience, location, and employer.

Is there a demand for medical writers?

There is strong demand for medical writers, especially those with expertise in clinical research, regulatory writing, and scientific communication. Remote medical writing consultants are sought after across pharmaceutical, biotech, and healthcare industries due to the need for clear, accurate documentation and regulatory submissions.

How can I make $70,000 a year working from home?

A remote medical writing consultant can earn $70,000 annually by building expertise in medical and scientific writing, obtaining relevant certifications, and gaining experience with pharmaceutical or healthcare companies. Developing strong research, writing, and editing skills, along with proficiency in tools like reference management software, can help increase earning potential. Consistent client relationships and specialization in high-demand areas also contribute to higher income levels.

Can you work from home as a medical writer?

Remote medical writing consultants can often work from home, as the role primarily involves creating and editing scientific documents, which can be done independently with a computer and relevant software. Many employers and freelance opportunities offer flexible, home-based arrangements, especially for experienced writers with strong research and communication skills.

Is content writing dead after Chatgpt?

For a remote medical writing consultant, AI tools like ChatGPT can assist with drafting and editing content, but they do not replace the need for specialized medical knowledge, accuracy, and compliance. Human expertise remains essential for creating high-quality, evidence-based medical documents, and content writing continues to evolve as a collaborative process between AI and professionals.

What is the difference between Remote Medical Writing Consultant vs Remote Medical Writer?

AspectRemote Medical Writing ConsultantRemote Medical Writer
CredentialsTypically requires advanced degrees (e.g., MD, PhD, PharmD) and industry certificationsOften requires a degree in life sciences or related field; certifications are a plus
Work EnvironmentConsults with clients, provides strategic guidance, and reviews documentsPrepares, writes, and edits scientific and regulatory documents
Employer & Industry UsageConsulting firms, pharmaceutical companies, CROsPharmaceutical, biotech, and healthcare companies

Remote Medical Writing Consultants focus on providing expert advice, strategic input, and review services, often working on complex projects. Remote Medical Writers primarily produce and edit scientific and regulatory documents. Both roles require strong scientific knowledge, but the consultant role emphasizes strategic oversight and client interaction, while the writer role centers on document creation and editing.

More about Remote Medical Writing Consultant jobs
What cities are hiring for Remote Medical Writing Consultant jobs? Cities with the most Remote Medical Writing Consultant job openings:
What are the most commonly searched types of Medical Writing Consultant jobs? The most popular types of Medical Writing Consultant jobs are:
What states have the most Remote Medical Writing Consultant jobs? States with the most job openings for Remote Medical Writing Consultant jobs include:
What job categories do people searching Remote Medical Writing Consultant jobs look for? The top searched job categories for Remote Medical Writing Consultant jobs are:
Remote Medical Writing Consultant jobs near you
Infographic showing various Remote Medical Writing Consultant job openings in the United States as of June 2026, with employment types broken down into 1% Locum Tenens, 72% Full Time, 23% Part Time, and 4% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $148,159 per year, or $71.2 per hour.
Senior Medical Writer (Remote)

Senior Medical Writer (Remote)

MMS Holdings Inc.

Canton, MI • On-site, Remote

Full-time

Posted 27 days ago

Job description

About MMS
MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating.
Our mission is to deliver high-quality service and technology solutions - rooted in strong science and decades of regulatory experience - that will assist our clients in developing and marketing life-changing therapies to positively improve lives worldwide.
MMS recognizes that a talented staff is what drives our business forward. Identifying and attracting top talent and continual training to strengthen core skills are essential to its core mission. At MMS, enthusiasm, collaboration, and teamwork are fostered, knowing that a global and diverse talent pool makes the company stronger. For more information, visit www.mmsholdings.com or follow MMS on LinkedIn.
Responsibilities
  • Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias
  • Write and edit clinical development documents, including but not limited to, clinical protocols, investigator's brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries, Module 2.7.1, 2.7.2, 2.7.3, 2.7.4, and 2.5 documents, presentation materials and publications to medical journals
  • Complete writing assignments in a timely manner
  • Maintain timelines and workflow of writing assignments
  • Practice good internal and external customer service
  • Highly proficient with styles of writing for various regulatory documents
  • Expert proficiency with client templates & style guides
  • Interact directly and independently with client to coordinate all facets of projects; competent communicator skills for projects
  • Contribute substantially to, or manages, production of interpretive guides
  • Take ownership of a given assignment, proactively consulting other project team members and other department representatives for information or guidance as necessary
  • Mentor medical writers and other members of the project team who are involved in the writing process
Requirements
  • At least 3 years of previous experience in the pharmaceutical industry
  • Must have at least 3-5 years of industry regulatory writing and clinical medical writing experience
  • The ideal candidate would hold a Bachelors, Masters, or Ph.D. in scientific, medical, clinical discipline
  • Substantial clinical study protocol experience, as lead author, required
  • Experience leading and managing teams while authoring regulatory documents with aggressive timelines
  • Experience in regulatory submissions (clinical study reports) presented to regulatory authorities a plus
  • Understanding of clinical data
  • Exceptional writing skills are a must
  • Excellent organizational skills and the ability to multi-task are essential prerequisites
  • Candidate must be an expert in MS Word, Excel, PowerPoint, and related word processing tools
  • Experience being a project lead, or managing a project team
  • Strong understanding of federal regulations, Good Clinical Practices, and ICH guidelines a plus
  • Not required, but experience with orphan drug designations and PSP/PIPs a plus

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