Clinical Research Physician

Added
18 days ago
Type
Full time
Salary
Salary not provided

Related skills

regulatory affairs china medical affairs clinical development kol

๐Ÿ“‹ Description

  • Frontline scientific expert for AbbVie China TA development
  • Provide clinical science insights for portfolio assessment, development plans, trial quality
  • Lead China local development project teams to propose strategies and pathways for new compound
  • Collaborate with Global JAPAC development teams, CDO, Regulatory Affairs, Medical Affairs, and
  • Ensure study design meets local regulatory requirements and enables efficient registration

๐ŸŽฏ Requirements

  • Medical Degree with 3+ years in medical/clinical development in pharma or equivalent
  • Understanding of regulatory development processes and cross-functional program interplays
  • Experience leading multiple clinical development programs
  • Strong study design, data handling, analysis, and interpretation skills
  • Excellent communication and collaboration with stakeholders
  • Patient-centric approach with compliance to relevant rules and quality standards

๐ŸŽ Benefits

  • AbbVie equal opportunity employer
  • Opportunity to work within a global development organization
  • Competitive compensation Grade 16 with hybrid work in Shanghai
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