Full Time


Posted 1 month ago
Application ends: November 4, 2021
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Job Description



  • Lead cross functional communication, finalize meeting presentations and takeaway messages, assign tasks and track deliverables against group decision
  • Support program leader and management team to drive decision, manage risk assessment and control, achieve milestones within timeline & budget, with comprehensive rational & prospective analysis & consolidated evidence
  • Liaison with cross functional teams to support program leader and management team to identify market setting, differentiate product SOWT matrix, manage progress adhere to corporate goal setting, make sure sufficient investigational product supply
  • Liaison with functional teams to fulfill requirement of regulatory submission, publications, protocol finalization, database lock, CSR finalization
  • Support program leader and management team to prepare documents for external collaboration negotiation
  • Participate cross functional communication, create necessary templates and documents to deliver results to meet sponsors’ & stakeholders’ expectations


Bachelor and above in chemistry, biology, medicinal training background

  • >3 years of related field experiences, CRO, biotech, or pharma
  • >3 projects completed with recognized deliverables, solid outcome and benefit to sponsors and stakeholders
  • >1 years of oncology, PK/PD, toxicology, formulation, process development & manufacturing, clinical trials related working experience
  • GLP, or ICH-GCP training working experience
  • Strong PM skills with solid training and recognized deliverables
  • Strong presentation skills with clear and persuasive logic, methodology, takeaway message
  • Mastering in PM tools is must
  • Fluent English and Chinese in both oral and written skills
  • Highly passionate and innovate, with outbox thinking spirit
  • Highly proactive with personal Objective setting and Key Results management