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Contract Scientific Writer Jobs in Raleigh, NC (NOW HIRING)

Kelly Services

Contract Technical Writer

Raleigh, NC · On-site

$40 - $47/hr

Contract Technical Writer - CAPA/SOP Remediation Location: Raleigh, NC (On-site) Pay Rate: $40-$47 ... Bachelor's degree in a scientific, technical, engineering, or communications-related field ...

Kelly Services

Contract Technical Writer

Raleigh, NC

$40 - $47/hr

Contract Technical Writer - CAPA/SOP Remediation Location: Raleigh, NC (On-site) Pay Rate: $40-$47 ... Bachelor's degree in a scientific, technical, engineering, or communications-related field ...

IQVIA

Site Contract Manager

Durham, NC

$86K - $115K/yr

Strong legal, financial and/or technical writing skills. * Strong understanding of regulated ... life sciences and healthcare industries. We create intelligent connections to accelerate the ...

IQVIA, Inc.

Site Contract Manager

Durham, NC · On-site

$86K - $115K/yr

Strong legal, financial and/or technical writing skills. * Strong understanding of regulated ... life sciences and healthcare industries. We create intelligent connections to accelerate the ...

IQVIA

Site Contract Manager

Durham, NC · On-site

$86K - $115K/yr

Strong legal, financial and/or technical writing skills. * Strong understanding of regulated ... life sciences and healthcare industries. We create intelligent connections to accelerate the ...

IQVIA

FSP Contract Negotiator

Durham, NC

Strong legal, financial and/or technical writing skills. Strong understanding of regulated clinical ... life sciences and healthcare industries. We create intelligent connections to accelerate the ...

IQVIA, Inc.

FSP Contract Negotiator

Durham, NC · On-site

... review of core scientific, technical and administrative documentation to support business ... writing skills. • Strong understanding of regulated clinical trial environment and knowledge of ...

IQVIA

FSP Contract Negotiator

Durham, NC · On-site

Strong legal, financial and/or technical writing skills. Strong understanding of regulated clinical ... life sciences and healthcare industries. We create intelligent connections to accelerate the ...

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Contract Scientific Writer information

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How much do contract scientific writer jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for contract scientific writer in Raleigh, NC is $45.80, according to ZipRecruiter salary data. Most workers in this role earn between $32.69 and $57.02 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a contract scientific writer?

To excel as a Contract Scientific Writer, you need strong scientific knowledge, excellent writing and editing skills, and typically a degree in a science or medical field. Familiarity with reference management software, document collaboration tools, and adherence to style guides like AMA or APA is often required. Attention to detail, time management, and the ability to communicate complex ideas clearly are important soft skills in this role. These competencies are crucial for producing accurate, high-quality scientific documents on deadline and collaborating effectively with researchers and clients.

What are typical challenges that contract scientific writers face in their daily work?

Contract Scientific Writers often juggle multiple projects with tight deadlines, requiring strong time management and organizational skills. Interpreting complex scientific data and ensuring accuracy while translating it into accessible content can be demanding. Additionally, writers must adapt quickly to each client's unique requirements and editorial standards, sometimes working with diverse teams of researchers or subject matter experts. Effective communication and a proactive approach to clarifying expectations with clients help mitigate these challenges and ensure successful project delivery.

What is a contract scientific writer?

A Contract Scientific Writer is a freelance or temporary professional who creates scientific documents, such as research articles, regulatory submissions, clinical study reports, and medical communication materials. They often work with pharmaceutical companies, research institutions, or healthcare organizations to translate complex scientific data into clear, accurate, and accessible content. This role requires strong writing skills, subject matter expertise, and the ability to adhere to industry guidelines. Contract arrangements allow flexibility in workload and project selection, making it an attractive option for experts in scientific communication.

What are the most commonly searched types of Scientific Writer jobs in Raleigh, NC? The most popular types of Scientific Writer jobs in Raleigh, NC are:
What are popular job titles related to Contract Scientific Writer jobs in Raleigh, NC? For Contract Scientific Writer jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Contract Scientific Writer jobs in Raleigh, NC look for? The top searched job categories for Contract Scientific Writer jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Contract Scientific Writer jobs? Cities near Raleigh, NC with the most Contract Scientific Writer job openings:
Contract Scientific Writer jobs near you
Infographic showing various Contract Scientific Writer job openings in Raleigh, NC as of August 2026, with employment types broken down into 73% Full Time, 9% Part Time, and 18% Contract. Highlights an 100% In-person job distribution, with an average salary of $95,269 per year, or $45.8 per hour.

Contract Technical Writer

Kelly Services

Raleigh, NC • On-site

$40 - $47/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 14 days ago

Job description

Contract Technical Writer – CAPA/SOP Remediation

Location: Raleigh, NC (On-site)
Pay Rate: $40–$47/hour
Engagement Type: Contract 
Schedule: Monday-Friday 8am-5pm
Duration: Initial 6–8 weeks with strong potential for extension
Openings: 3–4

Overview

We are seeking multiple Contract Technical Writers to support a high-priority documentation remediation initiative at a regulated manufacturing facility. This project focuses on reducing a backlog of CAPA-related documentation by updating and creating GMP-compliant technical documents. The team will work collaboratively with Quality, Manufacturing, and Laboratory personnel to ensure documentation meets regulatory and internal quality standards.

Responsibilities
  • Revise and update Standard Operating Procedures (SOPs) to support CAPA closure activities.
  • Author, revise, and format technical documentation, including batch records and laboratory forms.
  • Translate input from Quality, Manufacturing, and Laboratory subject matter experts into clear, compliant documentation.
  • Ensure all documents comply with cGMP requirements and internal quality systems.
  • Track assigned documentation against project timelines and CAPA due dates.
  • Collaborate with cross-functional teams to verify technical accuracy before document approval.
  • Utilize electronic document management and change control systems to draft, route, and maintain documentation.
Qualifications
  • Bachelor's degree in a scientific, technical, engineering, or communications-related field preferred; equivalent regulated manufacturing experience will be considered.
  • 3+ years of technical writing experience in a GMP-regulated pharmaceutical, biotech, medical device, or similar manufacturing environment.
  • Experience authoring and revising SOPs, batch records, work instructions, and laboratory documentation.
  • Working knowledge of CAPA processes, document control, and quality management systems.
  • Strong technical writing skills with an emphasis on clarity, consistency, and regulatory compliance.
  • Ability to work independently in a fast-paced, deadline-driven environment.
  • Proficiency with Microsoft Office and electronic document management systems.
Position Details
  • 3–4 contract openings available immediately.
  • Initial project expected to last 6–8 weeks, with a strong possibility of extension based on ongoing documentation needs.
  • This is a fully on-site position in Raleigh, NC.

As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice.

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