Technical Writer – 6-Month Contract (Fully Onsite)
Location: Morrisville, NC
Schedule: Monday–Friday, 8:00 AM – 5:00 PM
Pay Rate: $35–$45/hour
Type: 6-Month Contract (Fully Benefited)

We are seeking a Technical Writer for a fully onsite, 6-month contract position with full benefits. The ideal candidate will have experience creating and managing scientific and technical documentation in a regulated environment, particularly related to preclinical or clinical-stage drug development. This role will support cross-functional teams by preparing high-quality, accurate documentation that aligns with internal standards and regulatory expectations.

Key Responsibilities:

• Draft, edit, and format technical documents including study protocols, reports, SOPs, work instructions, and regulatory submissions

  
  

• Collaborate with scientific and operational teams to gather information and ensure content accuracy

  
  

• Maintain version control and document history in accordance with internal quality systems

  
  

• Ensure all documentation complies with applicable regulatory guidelines (GLP, GCP, etc.)

  
  

• Support audits and inspections by providing documentation as needed

Qualifications:

• Bachelor’s degree in a scientific or technical field required

  
  

• 3+ years of technical writing experience in biotech, pharma, or CRO settings

  
  

• Familiarity with regulatory documentation standards (GLP, GCP, FDA, ICH, etc.)

  
  

• Excellent written communication and organizational skills

  
  

• Must be comfortable working 100% onsite in Morrisville, NC

This is an excellent opportunity for a detail-oriented technical writer to contribute meaningfully to the development of life sciences programs in a collaborative, fast-paced setting.