Location: Beijing

Number of recruits:

Unlimited Responsibilities:

1. Responsible for developing clinical data management plan and data verification plan.

2. Responsible for CRF design, CRF annotation and guide of CRF fill;

3. Responsible for database construction, validation, testing, maintenance, guide data entry work, ensure data quality;

4. Data verification, data query management;

5. responsible for data medical coding.

6. Presided over data verification meetings, and wrote meeting reports;

7. Writing data verification report and data management report;

8. Perform other tasks related to data management.

Job requirements:

1. Familiar with ICH, GCP, GCDMP and other relevant laws and regulations for clinical trial data management.

2. Familiarity with data management procedures in clinical trials;

3. Have a certain EDC operating system and data management system operation experience with strong organizational planning ability, communication ability and analysis, problem-solving ability, thinking agile.

4. Have some experience in coding medical terminology, familiar with MedDRA and other coding tools.

5. with CDISC related experience, self-learning ability and strong initiative, and strive for continuous innovation;

6. Good communication ability, organizational ability, coordination ability, teamwork spirit, good sense of confidentiality and professional ethics.

7. Optimistic, open-minded, able to work under pressure and accept the necessary overtime work.