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Remote Biotech Technical Writer Jobs in Commack, NY

Nood

Technical Product Development Manager

New York, NY · Remote

$85K - $110K/yr

... devices, biotech, or consumer goods manufacturing * Experience owning launch timelines across ... Experience writing vendor and manufacturer communications independently, including technical ...

Heritage civil Works

Customer Support Specialist

New York, NY · Remote

$19.75 - $26.50/hr

... biotechnology, pollution control to energy innovation. Our clients depend on us not just for technical excellence, but for exceptional service. That's where you come in. We are looking for a Remote ...

Slang AI

Technical Recruiter (Contract)

New York, NY · On-site +1

$105K - $150K/yr

This is a fully remote role with occasional travel to company offsites and headquarters. You'll ... Strong written communication-your outreach, JDs, and candidate messages are clear, warm, and ...

Danaher

Filtration Sales Specialist

Stamford, CT · Remote

$100K - $130K/yr

... biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're ... The position is remote and is responsible for covering the Northeast US (New England), Quebec and ...

New

HiddenLayer

Technical Support Engineer

New York, NY · Remote

Technical Support Engineer Remote ABOUT THE ROLE: This is a unique opportunity to join HiddenLayer ... Clear, concise written communication (especially in high-pressure or ambiguous situations)

Classiq

Technical Product Marketing Manager

New York, NY · On-site +1

$182K - $211K/yr

Clear, concise writing and communication skills * Comfort working closely with engineers and ... Flexible, remote-friendly environment. * Shape quantum adoption in the US Federal landscape.

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All JobsBiotech Technical Writer JobsRemote Biotech Technical Writer JobsRemote Biotech Technical Writer Jobs in Commack, NY

Remote Biotech Technical Writer information

See Commack, NY salary details

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How much do remote biotech technical writer jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for remote biotech technical writer in Commack, NY is $40.33, according to ZipRecruiter salary data. Most workers in this role earn between $29.86 and $48.80 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a remote biotech technical writer?

To thrive as a Remote Biotech Technical Writer, you need a strong background in life sciences or biotechnology, excellent writing skills, and often a relevant degree or industry experience. Familiarity with scientific literature databases, document management systems, and regulatory writing standards such as ICH or FDA guidelines is typically required. Outstanding attention to detail, self-motivation, and the ability to communicate complex information clearly are vital soft skills. These abilities ensure the accurate, compliant, and accessible documentation that supports research, regulatory submissions, and internal communications in biotech organizations.

How does a remote biotech technical writer typically collaborate with scientists and subject matter experts while working off-site?

Remote Biotech Technical Writers often rely on virtual collaboration tools such as video conferencing, shared document platforms, and project management software to work closely with scientists and subject matter experts. Regular online meetings and clear communication channels are essential for clarifying complex scientific concepts, ensuring accuracy, and aligning on project goals. Writers may also participate in virtual lab tours or demonstrations to gain a deeper understanding of processes. Proactive communication and flexibility are key to overcoming time zone differences and ensuring high-quality deliverables.

What is the difference between Remote Biotech Technical Writer vs Remote Scientific Content Specialist?

AspectRemote Biotech Technical WriterRemote Scientific Content Specialist
CredentialsBiotech or life sciences degree, writing certificationsScience degree, content creation experience
Work EnvironmentRemote, biotech or pharma companiesRemote, research institutions or biotech firms
Employer UsageUsed in biotech, pharma, medical device industriesUsed in research, biotech, and educational sectors
Search & Comparison IntentUnderstanding technical writing roles in biotechComparing scientific content creation roles

The Remote Biotech Technical Writer focuses on creating clear, accurate documentation for biotech products, protocols, and regulatory submissions. The Remote Scientific Content Specialist, however, emphasizes developing scientific articles, educational materials, and marketing content. While both roles require a science background and strong writing skills, the technical writer is more regulatory and documentation-oriented, whereas the content specialist leans toward science communication and outreach.

What is a remote biotech technical writer?

A Remote Biotech Technical Writer is a professional who creates clear and accurate documentation related to biotechnology, such as research reports, regulatory submissions, standard operating procedures, and user manuals, while working from a location outside of a traditional office. They translate complex scientific information into understandable content for various audiences, including researchers, regulatory bodies, and the public. Remote Biotech Technical Writers often collaborate with scientists and regulatory experts using digital communication tools, allowing flexibility in their work environment. This role requires strong writing skills, attention to detail, and a solid understanding of biotech concepts and terminology.

What job categories do people searching Remote Biotech Technical Writer jobs in Commack, NY look for?

The top searched job categories for Remote Biotech Technical Writer jobs in Commack, NY are:

What cities near Commack, NY are hiring for Remote Biotech Technical Writer jobs?

Cities near Commack, NY with the most Remote Biotech Technical Writer job openings:

Remote Biotech Technical Writer jobs near you

Senior Medical Writer (Fixed-Term Contract)

COMPASS Pathways

New York, NY • On-site, Remote

$135K - $185K/yr

Full-time, Contractor

Posted 29 days ago

Job description

Company introduction:

Compass Pathways plc (Nasdaq: CMPS) is a biotechnology company dedicated to unlocking urgently needed new treatment options in mental health care.

The Company is headquartered in London, UK, with a U.S. office in New Jersey. We believe mental health patients deserve the possibility of a better future. Our initial focus is developing COMP360 psilocybin, a proprietary, investigational, synthetic psilocybin treatment under evaluation for treatment-resistant depression (TRD) and post-traumatic stress disorder (PTSD). COMP360 is a potentially first-in-class treatment and has Breakthrough Therapy designation from the U.S. Food and Drug Administration (FDA), as well as Innovative Licensing and Access Pathway (ILAP) designation in the UK for TRD.

We are leading the world's largest classic psychedelic clinical program in TRD, and building upon that robust foundation, we are executing a late-stage trial evaluating COMP360 for PTSD, another condition with high unmet need. Our goal is to advance treatments that move the field of psychiatry towards treatment options that offer rapid onset and sustained durability with infrequent dosing. - Compass Pathways

Job overview:

The Senior Medical Writer is responsible for developing various clinical regulatory documents related to our investigational product, our proprietary psilocybin therapy. This role leads document preparation, ensures adherence to regulatory and company standards, coordinates outsourced writing services, and collaborates with multidisciplinary teams to support the regulatory sciences function.

Location: Hybrid in our New York City office or remote on the east coast in the United States.

Reports to: Director, Medical Writing.

Duration: 6-month contract.

Roles and responsibilities
(Include but are not limited to):

  • Prepares and co-ordinates responses to regulatory agency information requests
  • Leads preparation of clinical regulatory documents, including CSRs, protocols, IB and clinical summaries (Module 2.7.x and ISE/ISS)
  • Ensures Compass clinical documents are clear, accurate, and written in accordance with the relevant guidance and best practice
  • Oversees and co-ordinates outsourced medical writing services as required
  • Provides subject matter expertise as a member of the regulatory sciences team
  • Accountable for compliance with ethical and scientific standards, regulatory requirements, and the Compass Quality Management System; ensuring participant safety, data integrity and accuracy throughout the trial process

Candidate profile:

  • Minimally a Bachelor's degree in the life or health sciences; MSc or PhD preferred
  • Experience in supporting regulatory submissions as a writer within the pharmaceutical industry/CRO
  • Experience in leading the development of clinical documents as part of a multi‑functional team, including CSRs, IBs, clinical summaries, ISS/ISE
  • Broad working knowledge of the clinical drug development process with experience of integrating information into clinical regulatory documents
  • Knowledge of relevant ICH guidance relating to clinical regulatory documentation
  • Excellent written English with aptitude for clear and concise writing
  • Excellent attention to detail and editorial skills
  • Flexibility in adapting to changing circumstances or new information
  • Alignment to our company culture and values

Compensation Description (annually):

Our compensation package for permanent hires includes base salary, discretionary bonus, and equity, alongside our comprehensive benefits offering.

Please note that the base salary range is a guideline, and individual total compensation will vary based on factors such as qualifications, skill level, competencies, and work location.

【Base salary per annum】:
$135,000—$185,000 USD
Benefits:

For an overview of our benefits package and compensation information, please visit "Joins us - Our Benefits".

These include flexibility & generous time off, parental & reproductive support, health & medical, mental health & wellbeing and Financial health.

Equal opportunities:

Reasonable accommodation
We are committed to building a workplace where everyone's wellbeing matters. If you need reasonable accommodation during the interview process to be at your best, please let our recruiting team know.

UK applicants

We are proud of our commitment to diversity and equality (pursuant to the Equality Act 2010). We do not discriminate based upon race, religion or belief, colour, nationality, ethnic or national origin, gender, pregnancy or maternity, marital or civil partner status, sexual orientation, gender reassignment, age or disability.

US applicants

Compass Pathways is proud to be an equal opportunity employer. All employment decisions are based on business needs, job requirements, and individual qualifications, without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, and related medical conditions), ethnicity, age, disability, sexual orientation, gender identity, gender expression, military service, genetic information, familial or marital status, or any other status, category, or characteristic protected by applicable law.

Sponsorship:

Unfortunately, we cannot sponsor employment visas and can only accept applications if you have employment rights in the country to which you are applying.

Data Privacy:

All data is confidential and protected by all legal and data privacy requirements, please see our recruitment Privacy Notice to learn more about how we process personal data.