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Remote Senior Medical Writer Jobs in Rochester, NY

Medical Writing Manager

Rochester, NY ยท Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project focused on ...

Medical Billing Specialist

Rochester, NY ยท Remote

$50 - $80/hr

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer's project focused on developing advanced AI-assisted writing tools for clinical documentation. In ...

Senior Counsel - Remote

Rochester, NY ยท Remote

$140 - $400/hr

Exceptional written and verbal communication skills, with demonstrated experience in legal content review. * Track record of successful remote collaboration and participation in multidisciplinary ...

Exceptional written and verbal communication skills, with demonstrated experience in legal content review. * Track record of successful remote collaboration and participation in multidisciplinary ...

Senior Environmental Engineer 1

Rochester, NY ยท On-site +1

$101K - $138K/yr

A remote position may be considered for the ideal candidate. DUTIES/RESPONSIBILITIES In this ... Excellent written and verbal communication skills to communicate with clients, senior project ...

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Remote Senior Medical Writer information

See Rochester, NY salary details

$34.5K

$135.5K

$244.2K

How much do remote senior medical writer jobs pay per year?

As of Aug 8, 2026, the average yearly pay for remote senior medical writer in Rochester, NY is $135,456.00, according to ZipRecruiter salary data. Most workers in this role earn between $102,600.00 and $163,800.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a remote senior medical writer, and why are they important?

A Remote Senior Medical Writer needs advanced scientific or medical knowledge, strong writing skills, and typically a relevant degree (e.g., life sciences, pharmacy, or medicine) with proven experience in medical communications. Familiarity with reference management tools, document management systems, and publication guidelines (such as ICMJE or GPP) is crucial. Exceptional attention to detail, time management, and the ability to communicate complex information clearly are standout soft skills. These competencies ensure the accurate, compliant, and timely delivery of high-quality medical documents vital for regulatory submissions, publications, and healthcare communications.

How does a remote senior medical writer typically collaborate with cross-functional teams while working off-site?

As a Remote Senior Medical Writer, you will regularly collaborate with medical, regulatory, and project management teams using virtual communication tools like video meetings, shared document platforms, and project management software. Clear and proactive communication is crucial, as you may need to bridge time zones and coordinate feedback from multiple stakeholders. While working remotely offers flexibility, it also requires strong organizational skills to manage deadlines and ensure your deliverables align with team objectives. Building strong relationships and maintaining transparency with your colleagues are key to ensuring smooth project progression and high-quality medical content.

What is the difference between Remote Senior Medical Writer vs Remote Medical Writer?

AspectRemote Senior Medical WriterRemote Medical Writer
CredentialsTypically requires advanced degrees (MD, PhD, PharmD) and experienceOften requires a relevant degree, such as life sciences or healthcare, with less experience needed
Work EnvironmentWorks independently or leads projects, often in a collaborative team settingSupports medical writing tasks under supervision, often in a team
Employer & Industry UsageUsed by pharmaceutical, biotech, and healthcare companies for complex documentationUsed across similar industries for standard medical content creation

The main difference between a Remote Senior Medical Writer and a Remote Medical Writer lies in experience, responsibilities, and credentials. Senior Medical Writers typically have advanced degrees and more experience, handling complex projects and leading teams. Medical Writers are often earlier in their careers, focusing on supporting documentation tasks under supervision. Both roles are vital in the healthcare and pharmaceutical industries, but the senior position involves greater expertise and leadership responsibilities.

What is a remote senior medical writer?

Remote senior medical writers are experienced professionals who create, review, and edit scientific and medical documents for pharmaceutical, biotechnology, or healthcare organizations while working from a remote location. Their work includes regulatory documents, clinical study reports, manuscripts, and educational materials. They ensure complex medical information is communicated clearly and accurately for both professional and lay audiences, and often collaborate with scientists, physicians, and regulatory teams. Senior medical writers typically have advanced degrees in life sciences and several years of writing experience.
What are popular job titles related to Remote Senior Medical Writer jobs in Rochester, NY? For Remote Senior Medical Writer jobs in Rochester, NY, the most frequently searched job titles are:
What job categories do people searching Remote Senior Medical Writer jobs in Rochester, NY look for? The top searched job categories for Remote Senior Medical Writer jobs in Rochester, NY are:
What cities near Rochester, NY are hiring for Remote Senior Medical Writer jobs? Cities near Rochester, NY with the most Remote Senior Medical Writer job openings:
Infographic showing various Remote Senior Medical Writer job openings in Rochester, NY as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution, with an average salary of $135,456 per year, or $65.1 per hour.

Medical Writer / Clinical Document Author

micro1 AI

Rochester, NY โ€ข Remote

$50 - $80/hr

Part-time

Posted 4 days ago


Job description

Role Title: Medical Writer / Clinical Document Author


Role Type: Contractor


Location: Remote


micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customerโ€™s project focused on developing advanced AI-assisted writing tools for clinical documentation. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required โ€” your domain knowledge is what matters.


Scope of Work

  1. Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development.
  2. Apply expert judgment to assess whether AI-generated content fulfills clinical template and structural requirements, including ICH E3 organization, section sequencing, cross-referencing, and appendix management.
  3. Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion, and conclusions, distinguishing true scientific or interpretive errors from stylistic differences.
  4. Trace narrative claims to source recordsโ€”tables, figures, listings, and protocolsโ€”to verify that all assertions are appropriately supported.
  5. Provide clear and structured written rationales for each assessment, enabling precise diagnosis and improvement of AI model behavior.
  6. Collaborate with project leads to refine evaluation frameworks and document best practices for clinical regulatory writing in the context of AI.


Preferred Qualifications

  1. Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent consultant.
  2. Direct experience independently authoring or leading the authoring of full Clinical Study Reports, beyond summaries or partial contributions.
  3. Fluency with ICH E3 and conventions for periodic safety documentation (ICH E2F, ICH E2C) and eCTD placement.
  4. Demonstrated ability to read and interpret TFLs and protocol documents, identifying where narrative diverges from source data.
  5. Exceptional written and verbal communication skills, especially in providing structured, actionable feedback on clinical content.
  6. Advanced degree in life sciences, pharmacy, or medicine (PhD, PharmD, MD, MSc), or equivalent depth of authoring experience.
  7. Experience across multiple clinical phases and therapeutic areas; oncology and haematology expertise is especially valued.


Join our customer's team and leverage your authoring expertise to help design the next generation of AI-assisted clinical documentation solutions. This high-bar role offers you the chance to shape how tomorrow's writing teams draft and review regulatory documents โ€” through your expert input, judgment, and real-world experience.