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Biotech Editor Writer Jobs (NOW HIRING)

STR

Biotechnology Principal Investigator

Woburn, MA · On-site

$220K - $280K/yr

About the Team STR is seeking a Biotechnology Principal Investigator (PI) to develop cutting-edge ... Technical proposal development (idea generation, writing, reviewing, editing) * Serve as primary ...

Precision AQ

Medical Writer, Medical Communications

Are you a team player - eager to partner with clients, editors, and scientific directors to get the ... biotech firms, we hold a leadership position in the delivery of strategic scientific and medical ...

Flywheel Partners

Medical Writer

Manhattan, NY · On-site +1

$65K - $85K/yr

We partner with pharmaceutical, medical device, and biotech companies to drive enhanced clinical ... Referencing, proofreading, and copy editing skills * High proficiency in Microsoft Word and ...

Flywheel Partners

Medical Writer

Manhattan, NY · Remote

$65K - $85K/yr

We partner with pharmaceutical, medical device, and biotech companies to drive enhanced clinical ... Referencing, proofreading, and copy editing skills * High proficiency in Microsoft Word and ...

Flywheel Partners, Llc

Medical Writer

Manhattan, NY · On-site

$80K - $85K/yr

We partner with pharmaceutical, medical device, and biotech companies to drive enhanced clinical ... Referencing, proofreading, and copy editing skills * High proficiency in Microsoft Word and ...

ATCC Biotechnology

Technical Writer

Manassas, VA · On-site

$68K - $75K/yr

This onsite position in Manassas, VA supports ATCC Federal Solutions by researching, organizing, writing, reviewing, and editing scientific and technical information for use in documentation across ...

Travere

Senior Manager, Medical Writing

San Diego, CA · On-site +1

Expert scientific writing, editing, and communication skills, with exceptional attention to detail ... biotechnology or pharmaceutical industry. * Knowledge of FDA, EMA, ICH, and other applicable ...

Travere

Senior Manager, Medical Writing

Expert scientific writing, editing, and communication skills, with exceptional attention to detail ... biotechnology or pharmaceutical industry. * Knowledge of FDA, EMA, ICH, and other applicable ...

Trident Consulting Inc

Medical Writer II

Aliso Viejo, CA · On-site

... biotechnology, pharmaceutical, or medical device industries. * Strong understanding of clinical ... Excellent writing, editing, proofreading, and organizational skills. * Strong attention to detail ...

AbbVie

Principal Strategic Medical Writer

Chicago, IL · On-site

A minimum of 5+ years of bio-pharmaceutical industry experience in a global pharma, biotech, life ... Extensive experience writing and editing clinical and regulatory documents following guidelines and ...

AbbVie

Principal Strategic Medical Writer

Chicago, IL · On-site +1

$109K/yr

A minimum of 5+ years of bio-pharmaceutical industry experience in a global pharma, biotech, life ... Extensive experience writing and editing clinical and regulatory documents following guidelines and ...

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Biotech Editor Writer information

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$37K

$84.5K

$130K

How much do biotech editor writer jobs pay per year?

As of Sep 10, 2026, the average yearly pay for biotech editor writer in the United States is $84,537.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,000.00 and $101,500.00 per year, depending on experience, location, and employer.

What are popular job titles related to Biotech Editor Writer jobs?

For Biotech Editor Writer jobs, the most frequently searched job titles are:

Infographic showing various Biotech Editor Writer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 91% Full Time, 1% Part Time, 1% Temporary, and 6% Contract. Highlights an 81% Physical, 5% Hybrid, and 14% Remote job distribution, with an average salary of $84,537 per year, or $40.6 per hour.

Medical Writer, Medical Communications

Remote

Precision Medicine Group
Pharmaceutical and Medicine Manufacturing • 1 - 5K employees
Learn more about Precision Medicine Groupexternal

Full-time

Posted 8 days ago

Job description

Are you a passionate individual that thrives when building scientific content designed to improve patient outcomes? Do you get excited when reviewing the most current research and can you interpret the science into action? We are proud to say that this is our core purpose.

Are you a team player - eager to partner with clients, editors, and scientific directors to get the job done? Then this dynamic role in medical communications is for you. Our interactive and dedicated team is committed to excellence and success.

We translate the science of medicine into high-level strategy, tactical communication, and flawless execution. With a track record of long-tenured relationships with major pharmaceutical companies and leading biotech firms, we hold a leadership position in the delivery of strategic scientific and medical communication and training solutions for our clients.

About you:

  • You have domain knowledge - knowledge of multiple therapeutic areas, regulatory/scientific guidelines, and key statistical concepts.
  • You know your audience and excel at maintaining data integrity.
  • You have excellent writing skills - logical and succinct with accurate data interpretation and representation.
  • You establish clear objectives, organize ideas and embrace creativity.
  • You conduct outstanding literature searches - using appropriate search strategy, keywords, and a variety of sources when researching journal articles, and medical research papers.
  • You're able to perform content reviews, correctly interprets results, identify potential limitations, and discusses unexpected findings.
  • Your interpersonal skills are well-honed verbal, nonverbal and listening skills for problem solving, negotiation and decision-making.
  • You are sought out by others - highly organized, dedicated, respects metrics driven timelines and accountability for quality.

What You Can Expect Day-to-Day:

  • You will generate content outlines that contain a clearly highlighted story arc and a complete reference list.
  • We will rely on you to develop client-ready drafts of content in various forms (slide decks, executive and comprehensive summaries, and other meeting materials).
  • We look forward to you organizing and annotating references in accordance with client's directives or house style.
  • We anticipate you will confer with the teams in the medical/legal/regulatory (MLR) review process, answering all queries from the MLR review committee, and understand and implement the required changes.

Qualifications

  • Advanced Science Degree (PharmD, MD, PhD) and 0-3 years of relevant experience
  • Proficiency in using Microsoft Word, PowerPoint, Excel, Adobe Acrobat, and reference-management software (e.g. EndNote)

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