Job Responsibilities:

1. Independently carry out all data management tasks related to the clinical trial;
2. Prepare data management-related documents, such as data management plans, data verification plans, and data management reports, among others;
3. Responsible for verifying and cleaning clinical trial data, as well as publishing and confirming the closure of queries in the database.
4. Responsible for SAS programming tasks, developing manual verification programs, and executing more complex medical logic checks.
5. Assist in extracting and exporting data from EDC;
6. Participate in completing medical coding tasks;
7. Responsible for organizing project operations, regularly reporting project progress, and preparing project progress reports.
8. Participate in completing the database lock (DBL) and subsequent data organization and submission;
9. Participating in the development of DM SOPs and systems;
10. Complete other tasks assigned by the company.

Job Requirements:

1. Bachelor's degree or higher; preference given to candidates with backgrounds in fields such as medicine, pharmacy, nursing, biostatistics, or related disciplines.
2. Has more than 1 year of experience in clinical trial data management;
3. Independently complete the full workflow of project data management for at least one project;
4. Strong logical thinking skills; interested in SAS programming (prior experience with SAS programming is preferred).
5. Possesses strong communication skills, as well as excellent organizational, coordination, and problem-solving abilities;
6. Diligent, meticulous, and patient in work; strong sense of responsibility.
7. Proficient in office software.

Inexperience can be developed.