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Entry Level Scientific Technical Writer Jobs in Raleigh, NC

MMS

Nonclinical Writer

Raleigh, NC · On-site

... meets scientific integrity * Ability to author based on highly technical sources such as GLP and ... Excellent written/oral communication and strong time and project management skills * Ability to ...

MDAEdge

LabWare LIMS-LES Developer

Raleigh, NC · On-site

... technical stakeholders. • Bachelor's degree in Computer Science, Life Sciences, or a related field. Preferred : • Experience with LabWare Pharma Template. • Knowledge of SQL and relational ...

North Carolina State University

Science Writer

Raleigh, NC · On-site

$65K - $75K/yr

The science writer is a key member of this team, translating the college's research and discoveries ... Distill complex academic, scientific, and technical research into compelling copy that can be ...

NCSU

Science Writer

Raleigh, NC

The science writer is a key member of this team, translating the college's research and discoveries ... Distill complex academic, scientific, and technical research into compelling copy that can be ...

Varsity Tutors

Technical Writing Tutor

Chapel Hill, NC · Remote

$18 - $40/hr

Emphasizes clarity, conciseness, and accuracy in conveying complex information and connects technical writing to software development, engineering, healthcare, and scientific communication ...

1001 Syneos Health, LLC

Proposal Writer

Raleigh, NC · On-site

Demonstrated ability to evaluate scientific and business information (e.g., clinical trial protocols) and use conclusions to write persuasive and technical sales documents. Intermediate to advanced ...

Icon plc

Senior Proposals Writer

Raleigh, NC · Remote

Bachelor's degree in life sciences, communications, or a related field. * Minimum of 2 years of experience in proposal writing, technical writing, or a similar role. * Excellent written and verbal ...

ICON

Senior Proposals Writer

Raleigh, NC · On-site

Bachelor's degree in life sciences, communications, or a related field. * Minimum of 2 years of experience in proposal writing, technical writing, or a similar role. * Excellent written and verbal ...

DataStaff, Inc.

Technical Recruiter

Raleigh, NC

DSI is currently in the process of interviewing entry-level professionals to join our award winning ... Excellent written and verbal communication skills are a must * Excellent PC skills required * Must ...

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Entry Level Scientific Technical Writer information

See Raleigh, NC salary details

$13

$37

$64

How much do entry level scientific technical writer jobs pay per hour?

As of Jul 26, 2026, the average hourly pay for entry level scientific 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 some common challenges faced by entry level scientific technical writers, and how can they overcome them?

Entry level scientific technical writers often face challenges such as translating complex scientific concepts into clear, accessible language for diverse audiences and adhering to strict formatting or publication guidelines. Working closely with subject matter experts can help clarify technical details, while seeking feedback from experienced writers or editors can improve clarity and accuracy. Building strong organizational skills and learning to manage multiple projects simultaneously are also key to success in this role.

What is the difference between Entry Level Scientific Technical Writer vs Scientific Communications Associate?

AspectEntry Level Scientific Technical WriterScientific Communications Associate
Required CredentialsBachelor's in Science, Technical Writing, or related fieldBachelor's in Science, Communications, or related field
Work EnvironmentResearch labs, biotech firms, scientific publishersResearch institutions, pharmaceutical companies, science media
Employer & Industry UsageUsed in scientific, biotech, and pharmaceutical sectorsCommon in science communication, media, and research organizations
Search & Comparison IntentYesYes

The Entry Level Scientific Technical Writer primarily focuses on creating clear, accurate technical documents for scientific audiences, often working closely with researchers. Scientific Communications Associates may have a broader role in science outreach, media, or public engagement. Both roles require strong scientific knowledge and communication skills, but their work environments and specific responsibilities differ slightly.

What are entry level scientific technical writers?

Entry level scientific technical writers are professionals who create clear and accurate documentation related to scientific topics, often for products, research, or technical processes. They typically work under the supervision of more experienced writers or scientists, translating complex scientific information into user manuals, reports, proposals, or online content. These writers need strong communication and writing skills, as well as a foundational understanding of scientific principles. Entry level positions often require a bachelor’s degree in a science or technical field, along with proficiency in written English. The role offers a pathway to more advanced technical writing or communications positions in science-focused industries.

What are the key skills and qualifications needed to thrive as an Entry Level Scientific Technical Writer, and why are they important?

To thrive as an Entry Level Scientific Technical Writer, you need a solid grounding in scientific principles, excellent written communication skills, and at least a bachelor's degree in a science or technical field. Familiarity with document management systems, Microsoft Office Suite, and sometimes basic knowledge of tools like LaTeX or Adobe Acrobat is typically required. Attention to detail, time management, and the ability to interpret complex information clearly are soft skills that set candidates apart. These competencies are crucial for accurately conveying technical information to diverse audiences and ensuring the clarity and compliance of scientific documentation.
What are the most commonly searched types of Scientific Technical Writer jobs in Raleigh, NC? The most popular types of Scientific Technical Writer jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Entry Level Scientific Technical Writer jobs? Cities near Raleigh, NC with the most Entry Level Scientific Technical Writer job openings:
Entry Level Scientific Technical Writer jobs near you
Infographic showing various Entry Level Scientific Technical Writer job openings in Raleigh, NC as of July 2026, with employment types broken down into 50% Internship, and 50% Full Time. Highlights an 100% In-person 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

Posted 27 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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