(Senior) Clinical Research Associate

Jan 11, 2022View PDF

Responsibilities:

  • Maintain clinical study sites.
  • Monitor and manage clinical study projects.
  • Keep accurate and complete records of clinical study data in compliance with protocols, GCP and SOPs requirements.
  • Follow up projects’ progress, solve different problems in clinical studies.
  • Other work assigned by line manager.

Qualifications:

  • Bachelor’s degree or above in Nursing, Clinical Medicine, Pharmacy or related majors.
  • At least 1 year’s experience in CRA. Familiarity with oncology projects will be a plus, especially with international multi-centers projects.
  • Good command of written and spoken skills, good coordination, planning and implementation ability.
  • A good team player with good moral virtue.
  • Familiar with GCP regulations and clinical related knowledge.