Clinical Trial Associate intern - TriArm

Key Responsibilities:

1. Responsible for organizing clinical trial data, including but not limited to ethical documents, trial data, and document management, according to the manager's requirements.
2. Supporting the execution of clinical trials at the hospital.
3. Proactively identify and manage risks and opportunities by offering simple, innovative solutions.
4. Through the internship, there is an opportunity to transition to a permanent position as a Clinical Research Associate (CRA) and conduct independent clinical trial monitoring work.