Senior Medical Writer

Job Summary

Leading the development and execution of medical writing strategies for clinical research projects, the full-time Senior Medical Writer will manage the preparation and review of clinical study documents, collaborate with cross-functional teams, and mentor junior writers, with the flexibility to work remotely or onsite.

Key responsibilities

• Oversee the preparation, review, and editing of clinical study documents, ensuring accuracy and clarity
• Collaborate with teams in clinical research, biostatistics, and regulatory affairs to analyze clinical trial data and summarize findings
• Participate in planning clinical development programs and contribute to publication plans for scientific dissemination

Required qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field
• Proficiency in interpreting complex clinical trial data and scientific research findings
• Strong understanding of regulatory requirements for clinical documents and experience with regulatory agencies
• Ability to manage multiple projects in a fast-paced environment while meeting deadlines
• Excellent interpersonal skills for effective collaboration with cross-functional teams