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

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