Clinical Research Physician

📋 Description 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