Clinical Research Physician

📋 Description

• Lead China local development efforts for AbbVie TA assets.
• Provide clinical science input for development plans and regulatory submissions.
• Coordinate with JAPAC, Global CDO, Regulatory, Medical Affairs, and cross-functional teams.
• Design development strategies and protocol discussions for China registration.
• Support trial safety, quality, and data review; enable efficient development tactics.

🎯 Requirements

• Medical Degree with ≥3 years in medical/clinical development in pharma or equivalent.
• Understanding of regulatory interplay and development programs.
• Strong data interpretation, study design, and scientific communication skills.
• Collaborative mindset with stakeholders and a patient-centric approach.
• Fluent English (spoken and written).

🎁 Benefits

• AbbVie equal opportunity employer information and company overview.
• Global development opportunities across JAPAC and China.
• Supportive environment with focus on innovation and scientific excellence.