Job Responsibilities:
1. Assist in pre‑study activities, project initiation, ethics submission, contract signing, and related tasks.
2. Serve as a liaison among the sponsor, CRO, investigators, and subjects to facilitate study progress.
3. Assist investigators in subject recruitment.
4. Assist in subject screening, enrollment, and follow‑up.
5. Assist in the collection, filing, submission, and management of study documents.
6. Perform clinical trial data entry and data query resolution.
7. Assist in the collection, centrifugation, storage, transport, and recording of biospecimens.
8. Assist investigators in AE recording and SAE reporting/documentation.
9. Assist in the management of investigational drugs.
10. Assist in study budget settlement and reimbursement.
11. Perform other tasks delegated by the Principal Investigator.
Requirements:
1. Associate degree or above (Bachelor’s degree preferred) in clinical medicine, nursing, pharmaceutical sciences, or a related field; at least one year of CRC experience with independent completion of at least one clinical trial.
2. Familiarity with relevant laws and regulations for drug/device clinical trials; hold a valid GCP training certificate.
3. Knowledge of hospital workflows; strong communication and coordination skills with investigators, site staff, and sponsors; strong execution ability.
4. Proficient in computer and office software; able to read literature both in Chinese and English.
5. Good team player, professional ethics, and dedication; proactive communication, meticulous, responsible, and able to work under pressure.
Salary: RMB 7,000 – 12,000 per month
HR Email: hr@cdwccr.com
