Nonclinical Regulatory Writer (Remote)

MMS; Seattle (WA); Remote; USD 70,000 - 85,000; Full time

Job summary

A clinical research organization is seeking an entry-level regulatory writer to join their innovative team in Seattle. This full-time, remote position involves developing and managing nonclinical documents while collaborating with cross-functional teams. Candidates should have a BS in a related field and 2+ years of nonclinical writing experience. The role offers a salary range of $70,000 to $85,000 along with a supportive work environment.

Qualifications

• 2+ years of pharmaceutical regulatory nonclinical writing experience.
• Proficiency with MS Office applications.
• Basic understanding of CROs and drug development process.

Responsibilities

• Develop and manage nonclinical documents.
• Lead projects independently with minimal oversight.
• Collaborate with cross-functional teams.

Skills

Regulatory writing

Analytical skills

Communication skills

Project management

Organizational skills

Team collaboration

Education

BS in pharmacology, toxicology, biology, or chemistry

Tools

MS Office

SharePoint

Veeva RIM

Job description

A clinical research organization is seeking an entry-level regulatory writer to join their innovative team in Seattle. This full-time, remote position involves developing and managing nonclinical documents while collaborating with cross-functional teams. Candidates should have a BS in a related field and 2+ years of nonclinical writing experience. The role offers a salary range of $70,000 to $85,000 along with a supportive work environment.