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MAKING SUCCESS STORIES HAPPEN
 

Responsibilities:
  • Coordinate and support multiple teams to ensure clinical trial operations run smoothly.
  • Facilitate effective communication across teams, including clinical sites, CROs, and company management.
  • Engage with CRA/CPM from contracted CROs and Principal Investigators/Site Coordinators at clinical sites to optimize patient recruitment strategies.
  • Conduct routine monitoring of clinical sites and contracted CROs to oversee proper PK/PD sample collection and analysis processes.
  • Compile, analyze, and summarize clinical data to create comprehensive reports.
  • Handle additional tasks as assigned by the supervisor.
Qualifications:
  • Academic background in biomedical sciences or related fields. Proven experience (3-4 years) in clinical operations or research, particularly within new drug development studies.
  • Strong organizational skills to manage study data, reports, documentation, and records.
  • Demonstrated adaptability and eagerness to acquire new skills and knowledge relevant to project needs.
  • Proficiency in communication and interpersonal skills.
  • Foundational skills in report writing and presentations.

 
Apply for Clinical Project Manager
Reference: GC865215

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Clinical Project Manager
Taipei, Taiwan | Permanent