Frontline scientific expert for AbbVie TA development in China
Lead China local development projects and protocol discussions
Collaborate with Global JAPAC, CDO, Regulatory, Medical Affairs, and Commercial teams
Ensure study safety and quality; support regulatory submissions
Establish partnerships with Chinese academia and study centers
Provide medical training to CDO and investigators

🎯 Requirements

Medical degree with TA expertise
≥3 years in medical/clinical development in pharma
Strong understanding of regulatory and development processes
Experience in study design, data analysis, and regulatory documents
Excellent communication and collaboration skills
Fluent English, both written and spoken

🎁 Benefits

AbbVie equal opportunity employer
Global development exposure
Hybrid work model in Shanghai

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