Clinical Research Associate

1. Research center screening Start up;

2. Provide ongoing training to center personnel on GCP, research plans, and requirements;

3. During the initiation and conclusion stages of the research, collect necessary documents in a timely manner according to the requirements of the plan and regulations, and update the researcher folder and TMF in a timely manner;

4. Conduct clinical monitoring work according to the company's SOP and be responsible for managing the entire process of clinical trials;

5. Ensure that the experiment strictly follows the plan GCP and related laws and regulations implementation;

6. Assist in resolving potential issues that may arise during the experimental process;

7. Ensure timely research data Accurate Integrity;

8. Responsible for the operation and execution of clinical projects according to the project plan and schedule, ensuring that the clinical projects are completed as required;

9. Assist in organizing various meetings related to clinical trials, maintain good communication and coordination with research units and experts

1. Bachelor's degree or above, major in medicine or related fields;

2.1 years or more of CRA work experience or 2 years or more of CRC experience in cancer projects;

3. Strong communication skills, planning ability, and organizational coordination ability; Passionate, outgoing, dedicated to work, hardworking, and organized Strong discipline;

4. Ability to independently face complex environments, courage to take responsibility, strong initiative and self-development skills Can adapt to long-term business trips and high-intensity work;

5. Have a certain level of English reading and writing ability, good computer and network application skills, and strong comprehensive work ability;

6. Base location: Beijing Suzhou Hefei Shenzhen