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.