Key skills
AI
About this role
Role Overview
- Drafting and managing reviews of submission documents for nonclinical pharmacology and toxicology
- Collaborating with scientists to interpret data and develop key messaging
- Authoring and managing internal reviews of nonclinical study reports
- Driving documents through comment reconciliation among key stakeholders
- Advancing multiple projects while adhering to submission timelines
- Participating in process improvement and training junior writers
Requirements
- 6+ years with BS or MS in Life Sciences-related field
- 2+ years with PhD in a Life Sciences-related field
- Experience with eCTD and drug development process
- Strong attention to detail, time-management skills, and scientific rigor
- Proficiency in Word, Excel, Adobe, GraphPad Prism
- Basic job-relevant AI experience
- Fluent in English.
Benefits
- health and wellness programs (including medical, dental, vision, life, and disability insurance)
- fitness centers
- 401(k) company match
- family support benefits
- equity awards
- annual bonuses
- paid time off
- paid leaves (e.g., military and parental leave) for eligible employees at all levels!