Sr Clinical Research Physician

Added
2 hours ago
Type
Full time
Salary
Salary not provided

Related skills

china regulatory submissions medical affairs clinical development kol
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๐Ÿ“‹ Description

  • Lead China local development project team to propose development strategies for new compound
  • Design clinical development plans and protocol discussions to meet local regulatory requirements.
  • Coordinate with Global JAPAC, CDO, Regulatory Affairs, Medical Affairs, and Commercial Development
  • Manage medical activities such as medical surveys, Ad Board meetings, and KOL visits to support
  • Support regulatory submissions and provide clinical expertise for successful approvals in China.

๐ŸŽฏ Requirements

  • Medical degree with 3+ years in medical/clinical development in pharma/biopharma or equivalent
  • Understanding of regulatory framework and cross-functional program development in Clinical
  • Experience in study design, data collection/analysis/interpretation, and ability to summarize data
  • Strong communication, collaboration, and patient-centric mindset with high ethical standards.
  • Fluent spoken and written English.

๐ŸŽ Benefits

  • AbbVie equal opportunity employer.
  • Opportunity to work with leading teams in Immunology & Aesthetics in China.
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