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Biotech Technical Writer Jobs in Raleigh, NC (NOW HIRING)

MMS

Nonclinical Writer

Raleigh, NC · On-site

We support the pharmaceutical, biotech, and medical device industries with our proven, scientific ... This person will participate in the development, writing, and management of highly technical non ...

Capstone Search Partners

Patent Agent

Raleigh, NC · On-site

$110K - $210K/yr

S. and international patent applications in the life sciences sector, including biotechnology ... Excellent technical writing and analytical skills with a keen attention to detail. * Ability to ...

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Biotech Technical Writer information

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$13

$37

$64

How much do biotech technical writer jobs pay per hour?

As of Jul 13, 2026, the average hourly pay for biotech technical writer in Raleigh, NC is $37.86, according to ZipRecruiter salary data. Most workers in this role earn between $28.03 and $45.82 per hour, depending on experience, location, and employer.

What are the common challenges faced by Biotech Technical Writers in their daily work?

Biotech Technical Writers often encounter the challenge of translating highly technical and complex scientific data into clear, concise documents for diverse audiences, including regulatory agencies and non-specialist stakeholders. They must stay up-to-date with evolving regulations and industry best practices, which can be demanding in a rapidly changing biotech landscape. Additionally, working closely with subject matter experts from research, development, and regulatory teams requires strong collaboration and communication skills to ensure accuracy and consistency. Overcoming these challenges not only sharpens your abilities but also makes you an invaluable asset within interdisciplinary biotech environments.

What are the key skills and qualifications needed to thrive in the Biotech Technical Writer position, and why are they important?

To thrive as a Biotech Technical Writer, you need a solid understanding of scientific concepts, excellent written communication skills, and often a degree in life sciences, biotechnology, or a related field. Familiarity with document management systems, scientific publishing software, and regulatory compliance guidelines such as Good Laboratory Practices (GLP) or FDA requirements is typically required. Strong attention to detail, adaptability, and the ability to collaborate with cross-functional teams are essential soft skills in this position. These competencies are crucial for effectively translating complex scientific content into clear, accurate documentation that supports research, product development, and regulatory submissions.

What is a Biotech Technical Writer job?

A Biotech Technical Writer creates clear, accurate, and concise documentation related to biotechnology, such as research reports, regulatory submissions, standard operating procedures (SOPs), and product manuals. They translate complex scientific concepts into understandable content for various audiences, including researchers, regulators, and the general public. This role requires strong writing skills, attention to detail, and knowledge of biotech terminology and industry regulations. Biotech Technical Writers often collaborate with scientists, engineers, and regulatory professionals to ensure documentation meets industry standards.

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What cities near Raleigh, NC are hiring for Biotech Technical Writer jobs? Cities near Raleigh, NC with the most Biotech Technical Writer job openings:
Biotech Technical Writer jobs near you
Infographic showing various Biotech Technical Writer job openings in Raleigh, NC as of July 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 83% In-person, and 17% Remote job distribution, with an average salary of $78,739 per year, or $37.9 per hour.
Nonclinical Writer

Nonclinical Writer

MMS

Raleigh, NC • On-site

Full-time

Re-posted 15 days ago

Job description

Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.
Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn.
This person will participate in the development, writing, and management of highly technical nonclinical documents. This is a full-time, remote position. 
Roles and Responsibilities:
  • Strong experience with development and writing of nonclinical documents (eg, Module 2.4 and 2.6 eCTD submission documents, Investigator’s Brochure [IB], Nonclinical Study Reports, Meeting Requests, Briefing Documents, RTQs)
  • Lead projects independently with minimal oversight, lead the writing (structure, content and messaging) of nonclinical documents, ensure the nonclinical package aligns with current regulatory guidelines and meets scientific integrity
  • Ability to author based on highly technical sources such as GLP and non-GLP nonclinical study reports, in vivo and in vitro nonclinical data
  • Ability to develop a mapping plan for the placement of nonclinical studies within structure of Module 2.4 and 2.6 eCTD submission documents
  • Interpret and analyze applicable pharmacokinetics, pharmacology, and toxicology data (eg, Prism files, bioanalytical reports, clinical pathology reports, PK/TK evaluation reports)
  • Collaborate with cross-functional teams such as project management, safety, efficacy, biostats, regulatory operations, and CMC
  • Demonstrated ability to lead others to complete complex projects
  • Ability to complete documents according to sponsor’s format, processes, and according to regulatory guidelines
  • Ability to effectively operate in an environment that requires negotiation, persuasion, collaboration, and analytical judgment
  • Organizational expert within the nonclinical subject area
  • Excellent written/oral communication and strong time and project management skills
  • Ability to attend regular team meetings, lead client meeting and CRMs
  • Ability to work in various client systems (eg, SharePoint, Veeva RIM, PleaseReview, EndNote), templates and toolbars
  • Strong understanding of regulatory guidances as it applies to nonclinical submission documents and drug development (eg, ICH, FDA and EMA regulations and guidelines, GLP, GCP, GMP and GDP)
Requirements:
  • BS + in pharmacology, toxicology, biology or chemistry, or related field, with industry experience within regulatory writing, regulatory affairs, laboratory sciences, quality assurance/control
  • Knowledge of GLP, ICH guidelines, and applicable regulatory requirements
  • 2+ years of pharmaceutical regulatory nonclinical writing experience
  • Strong writing and analytical skills
  • Proficiency with MS Office applications.   
  • Hands-on experience with clinical trial and pharmaceutical development preferred
  • Basic understanding of CROs and scientific & nonclinical data/terminology, & the drug development process

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About M. M. S.

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1 - 10 Employees

Headquarters location

Los Angeles, CA, US

Year founded

1980

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