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Freelance Scientific Technical Writer Jobs (NOW HIRING)

Houston Methodist

Six years' experience in technical or scientific writing * Two years with grant applications preferred LICENSES AND CERTIFICATIONS Required * SKILLS AND ABILITIES * Demonstrates the skills and ...

Accelint Holdings LLC

Technical Writer

San Diego, CA · On-site

$78 - $98/hr

Bachelor's degree in Engineering, Computer Science, Technical Communication, or a related field (or equivalent practical experience). Clearance Requirements Some positions will require access to U.S.

New

Eurofins

Technical Writer

Lenexa, KS · On-site

Company Description Eurofins Scientific is an international life sciences company, providing a ... The BioPharma Technical Writer is responsible for developing, reviewing, and maintaining controlled ...

Lyntris

Technical Writer

San Diego, CA · On-site

$78 - $98/hr

Bachelor's degree in Engineering, Computer Science, Technical Communication, or a related field (or equivalent practical experience). Clearance Requirements Some positions will require access to U.S.

New

Synerfac Technical Staffing

Technical Writer

Whippany, NJ · On-site

$45 - $50/hr

Communication - Strong technical writing and editing skills; ability to translate complex, technical, or scientific input into clear, concise procedures and records. * Detail Oriented - Ability to ...

Houston Methodist

Six years' experience in technical or scientific writing * Two years with grant applications preferred LICENSES AND CERTIFICATIONS Required * SKILLS AND ABILITIES * Demonstrates the skills and ...

Synerfac Technical Staffing

Technical Writer

Whippany, NJ · On-site

$45 - $50/hr

Communication - Strong technical writing and editing skills; ability to translate complex, technical, or scientific input into clear, concise procedures and records. * Detail Oriented - Ability to ...

Apogee Engineering, LLC

Technical Writer

Bedford, MA · On-site

$100 - $120/hr

Prepare original technical papers, manuals, policies, specifications, and reports in scientific, technical, or professional fields. * Write and edit user documentation, how-to guides, instruction ...

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How much do freelance scientific technical writer jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for freelance scientific technical writer in the United States is $23.27, according to ZipRecruiter salary data. Most workers in this role earn between $20.43 and $26.20 per hour, depending on experience, location, and employer.

What is a freelance scientific technical writer?

A Freelance Scientific Technical Writer is a professional who specializes in creating clear, accurate, and well-structured scientific documents on a contract or project basis. They often work with researchers, scientists, and organizations to write research articles, grant proposals, manuals, reports, and other technical materials. Unlike staff writers, freelancers operate independently and may serve multiple clients simultaneously. Their work helps communicate complex scientific information to both expert and non-expert audiences. Strong writing skills, subject matter expertise, and the ability to translate technical data into accessible language are essential for success in this role.

How do freelance scientific technical writers typically collaborate with subject matter experts during a project?

Freelance Scientific Technical Writers often work closely with subject matter experts (SMEs) such as researchers, clinicians, or engineers to ensure technical accuracy and clarity in their documents. This collaboration usually involves conducting interviews, reviewing drafts together, and clarifying complex scientific concepts. Communication is often handled via email, video calls, or collaborative platforms, requiring the writer to be proactive in scheduling meetings and asking precise questions. Building strong relationships with SMEs helps streamline the review process and produce high-quality, accurate scientific content.

What are the key skills and qualifications needed to thrive as a freelance scientific technical writer, and why are they important?

A Freelance Scientific Technical Writer needs a solid background in science or engineering, excellent writing skills, and often a relevant degree or equivalent experience. Familiarity with reference management tools, document formatting software (such as Microsoft Word or LaTeX), and sometimes certification from organizations like the American Medical Writers Association is highly beneficial. Outstanding attention to detail, the ability to communicate complex ideas clearly, and strong time management set top professionals apart. These skills and qualifications ensure accuracy, clarity, and reliability in scientific communication, which is critical for informing research, regulatory, or public audiences.
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Freelance Scientific Technical Writer jobs near you
Infographic showing various Freelance Scientific Technical Writer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 89% Full Time, 6% Part Time, 3% Contract, and 1% Nights. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution, with an average salary of $48,412 per year, or $23.3 per hour.

FSP Senior Scientist-Scientific Writer

Thermo Fisher Scientific

Collegeville, PA • On-site

Full-time

Posted 3 days ago

New

Thermo Fisher Scientific rating

7.8

Company rating: 7.8 out of 10

Based on 428 frontline employees who took The Breakroom Quiz

175th of 543 rated manufacturers

Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
This is a fully onsite role based at our customer's site in Collegeville, PA We welcome applicants from all locations within the US. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate.
Must be legally authorized to work in the United States without sponsorship.
Must be able to pass a comprehensive background check, which includes a drug screening.
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
Within our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to leverage the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits.
Summarized Purpose:
Testing of clinical biological samples for various biomarkers using immunoassay platforms (MSD, Quanterix, etc.) in a GCP compliant environment.
Essential Functions:
  • Develop and validate immunoassay methods to support clinical biomarker endpoints.
  • Prepare regulated documents, including validation plans and reports, analytical reports, and SOPs.
  • Perform routine testing of clinical biological samples (primarily serum) to support biomarker analysis using validated immunoassay methods in a Good Clinical Practice (GCP) compliant laboratory.
  • Execute assays on immunoassay platforms such as Meso Scale Discovery (MSD) and similar technologies (e.g., Quanterix), following established standard operating procedures (SOPs).
  • Prepare, handle, and process clinical samples in accordance with laboratory safety procedures and biohazard handling guidelines.
  • Conduct testing using validated methods with minimal method development responsibilities, ensuring data quality, accuracy, and adherence to study timelines.
  • Document all laboratory activities clearly and contemporaneously in compliance with GCP, internal quality standards, and regulatory requirements.
  • Review assay results for accuracy and completeness; identify routine technical issues and escalate concerns appropriately.
  • Support clinical study workflows including sample receipt, tracking, preparation, analysis, and data reporting.
  • Assist with assay validation activities and laboratory investigations as assigned.
  • Maintain laboratory equipment, reagents, and consumables to ensure operational readiness and inspection readiness.
  • Collaborate with team members to meet project milestones and contribute to a compliant, organized laboratory environment.

Education and Experience:
Bachelor's degree in related area with 2+ years of experience in a regulated bioanalytical laboratory.
In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role
Knowledge, Skills, and Abilities:
Immunoassay experience and experience with Watson LIMS preferred.
Why Join Us?
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You'll work in an environment where collaboration and development are part of the everyday experience - and where your contributions truly make a difference.
Apply today to help us deliver tomorrow's breakthrough.

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