Manager, Clinical Operations


Department: Clinical Operations

Purpose of Job: Clinical Operation Manager is accountable for trial delivery with high quality, and within timeline and budget

Major Responsibilities

  • Plan, organize, and manage all aspects of assigned clinical trial programs to ensure the clinical trial is conducted with good quality within approved timeline and budget
  • Work with BeiGene team and/or CRO (if applicable), to establish timelines and budget for the project
  • Lead and manage the efforts of all key functional departments to perform all project-related activities according to project milestones/timelines
  • Communicate with internal and external staff effectively with professional and collaborative approach. Escalate issues to BeiGene Senior Management team timely
  • Demonstrates strong initiative in activities through the clinical trials and other company initiatives
  • Proactively identify potential issues and seek improvement. Take initiative for issue resolution within and outside clinical department. Coordinate the risk management process encompassing proactive risk identification, evaluation (probability and impact) and mitigation plans
  • Contribute to strategy planning by bringing operational expertise
  • Demonstrates active training and mentoring of others
  • Provide ongoing mentoring and training to project team and other individuals, as appropriate
  • Perform quality oversight visit, if require
  • Take accountability and ownership for tasks within the job description, and other tasks assigned according to business needs
  • Being a team player and help others when require


  • Bachelor’s level degree or above in life sciences, pharmacy, nursing or medical
  • Five or more years of clinical research experience in the Pharmaceutical or CRO industry
  • Demonstrated strong project management capabilities and capable of training / mentoring others
  • Demonstrated experience working on a team across multiple functional areas
  • Knowledgeable expert in the execution of clinical trials, expert understanding of GCP/ICH Guidelines and other applicable regulatory requirements
  • Excellent communication, relationship building and interpersonal skills
  • Excellent organizational skills and ability to prioritize and multi task
  • Fluent in English (writing and speaking)

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