Late Phase Medical Writer at Syneos Health

Elevate your career with Syneos Health as a Senior Medical Writer, focusing on late-phase regulatory documentation. Utilize your skills in CSR and protocol writing to steer impactful changes in the medical writing landscape. This role demands your experience in drafting significant regulatory submissions like IND and NDA. You'll collaborate with various teams while guiding less experienced writers through complex projects, upholding high standards of regulatory compliance and fostering improvement. Key Responsibilities:

• Author protocols and clinical study reports
• Manage coordination of writing tasks among departments
• Ensure adherence to regulatory compliance
• Perform document reviews for precision
• Enhance internal writing processes

Requirements:

• Proven experience in writing clinical documentation
• Strong understanding of ICH regulatory guidelines
• Excellent editing and review skills
• Build collaborative relationships effectively
• Work successfully within set project timelines and budgets

Bring your expertise in medical writing to Syneos Health and support the advancement of late-phase studies. #J-18808-Ljbffr