Clinical Research Physician
AbbVieShanghaiFull TimeHealthcare
Remotely
medical affairsregulatory affairsclinical developmenttrialchinaprotocolkolregistration
Job Description
📋 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.
