Nonclinical Medical Writer

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

Mar 4, 2025 - 00:13

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