Job description

1. Responsible for quality assurance of clinical trials to ensure compliance with GCP specifications;
2. Review clinical quality system documents;
3. Take charge of random inspection of archived records related to clinical trials and supervision of drugs used in clinical trials;
4. Participate in the audit of the clinical site, and track the rectification of the audit report;
5. Complete other tasks assigned by the superior.

Job requirements

1. Bachelor degree or above in biology, chemistry, pharmacy or other related majors;
2. At least 2 years of QA experience in pharmaceutical production or R&D, or more than 2 years of experience in clinical trials;
3. Have GMP or GCP training experience;
4. Good at learning, strong sense of responsibility, good communication skills, and good team spirit;
5. Experience in quality management of clinical CRO company is preferred.