Your Role:

• • Conduct clinical assessments and manage study participants according to protocol.
• • Ensure adherence to ethical and regulatory requirements.
• • Collaborate with research staff and investigators for smooth project implementation.
• • Prepare and review clinical documentation and reports.

Must have:

• • Medical degree and valid PRC license.
• • Experience in clinical research or hospital practice preferred.
• • Knowledge of Good Clinical Practice (GCP) guidelines.
• • Strong analytical, communication, and decision-making skills.