Medical Writer - Senior Regulatory Writing Specialist (Clinical)

Medical Writer - Senior Regulatory Writing Specialist (Clinical) 

Essentials:

• 3+ years of regulatory writing experience (actual writing, not just a contributor)
• Experience with at least 3 different regulatory documents (including but not limited to: clinical study reports, protocols, Investigators Brochures, briefing documents, Module 2 documents)
• Client-facing experience/project management experience
• Excellent attention to detail MS Word expertise
• Experience with quality control (QC) review
• Fluent: C1 or C2 - English language
• Clinical regulatory experience
• Location: Remote Brazil

Nice-to-Have:

• PhD, PharmD, or MD
• Nonclinical (or preclinical) writing experience (Module 2.4 or Module 4 documents)
  
• Science or research experience (PhD/PharmD not required, but s...