Clinical Supervisor

1.Screening and initiation of study centers.

2.Provide ongoing training to center personnel on GCP, study protocols and requirements.

3.Collect necessary documentation and update investigator folders and TMF in a timely manner according to protocol and regulatory requirements during the initiation and completion phases of the study.

4.Perform clinical monitoring according to company SOPs and manage the entire process of clinical trials.

5.Ensure that the trial is conducted in strict accordance with the protocol, GCP and relevant laws and regulations.

6.Assist in solving any problems that may arise during the trial.

7.Ensure the study data is timely. Accuracy. Integrity.

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

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

1.Bachelor's degree or above, majoring in medicine or related field.

2.1 years of CRA work experience or 2 years of CRC experience in oncology projects.

3.Good communication skills, planning skills, organization and coordination skills; enthusiastic, cheerful, dedicated, hard-working, organized. Strong discipline.

4.Have the ability to face the complex environment independently, the courage to take responsibility, with strong initiative and self-development ability. Able to adapt to long-term travel and high intensity work.

5.Have certain English reading and writing skills, good computer and network application skills, and good overall working ability.

6.base location: Beijing. Suzhou. Hefei. Shenzhen