Principal Research Scientist II, Toxicology

📋 Description

• Oversee China-based CRO nonclinical toxicology studies and support development programs in China.
• Coordinate with AbbVie US stakeholders throughout study lifecycle.
• Prepare documentation for regulatory submissions (briefing books, CTDs) and provide regulatory
• Collaborate with US DBS development reps to ensure alignment across programs.
• Location in China with travel to CROs/regulatory sites as needed.

🎯 Requirements

• PhD, DVM or MD required.
• ≥10 years in pharmaceutical nonclinical safety leadership.
• Experience in regulatory documents for China; GLP knowledge and practices.
• Familiar with global guidance including US/EMA; bilingual Chinese/English.
• Strong timeline/project management; proficient with MS Office.

🎁 Benefits