Senior Medical Writer

We are seeking an experienced Senior Regulatory Medical Writer to lead authoring and development of high complexity clinical regulatory documents. The ideal candidate will have a background in life sciences and a minimum of 4 years of regulatory medical writing experience, including 2 years as a medical writing project lead.

Requirements

• Advanced degree in life sciences (PhD or Masters)
• Minimum 4 years of regulatory medical writing experience, including at least 2 years as medical writing project lead
• Extensive experience and proficiency in writing and leading development of CSRs and Protocols
• Excellent communication skills
• Ability to lead team discussions, manage complex medical writing tasks and processes, and engage with a variety of stakeholders

Benefits

• Comprehensive training
• Management support
• Network of SMEs and KOLs
• Opportunities to help employees thrive