Nonclinical Medical Writer

Job Summary

A company is looking for a Nonclinical Medical Writer (Part Time).

Key Responsibilities

• Develop and manage nonclinical regulatory writing deliverables and documentation
• Coordinate and author nonclinical regulatory documents, ensuring integration of scientific and regulatory input
• Participate in IND or CTA subteams, managing timelines and document organization

Required Qualifications

• 7 years of experience in the research medical pharmaceutical or biotechnology industry
• Minimum of 5 years as a medical writer preparing regulated documents, particularly in oncology or rare diseases
• Technical expertise in Microsoft Office and Adobe Acrobat; familiarity with document management systems
• Good understanding of global pharmaceutical drug development and regulatory submission requirements
• Bachelor's degree required; advanced degree preferred