Senior Medical Writer

Senior Medical Writer job at ProPharma Group involves writing high-quality medical writing deliverables, supervising junior writers, and adhering to regulatory standards. The role requires advanced knowledge of clinical research principles, strong project management skills, and exceptional communication skills. The ideal candidate will have a minimum of 5 years of experience in writing clinical and/or regulatory documents for drugs, biologics, and/or medical devices/diagnostics.

Requirements

• Write high-quality medical writing deliverables
• Supervise and mentor junior medical writers
• Adhere to established regulatory standards/guidelines
• Manage client expectations and interact with clients
• Interact and collaborate with subject matter experts
• Perform QC reviews and maintain audit trails
• Review statistical analysis plans and table/figure/listing shells
• Perform peer review of documents
• Assist with project-related administrative tasks

Benefits

• Generous Paid Time Off
• 401k Matching
• Retirement Plan
• Relocation Assistance