| Specific requirements: | Job Function : Clinical Coordinator Clinical Fellow Job Description : Responsibilities: 1. Write clinical trial plans and single disease clinical research plans; 2. Drafting registration application materials; translation of clinical trial documents; 3. Carry out comprehensive supervision and liaison management of the research center, and complete the start, execution and termination of clinical trials in the center on time;
4. Responsible for the coordination, supervision and quality control of clinical trial hospitals, progress supervision, reporting, Document management, etc.;
5. Check and report the progress and quality of the trial, fill in the case report form, adverse reactions and other aspects, find problems, analyze problems, propose solutions and implement them;
6. Regularly summarize and submit monitoring reports; fill in relevant Reports and test records to ensure that the data is true, accurate and complete;
7. Communicate with clinicians and jointly negotiate to solve problems that arise, and coordinate the relationship between the research project leader, clinicians, auxiliary departments and other parties; 8. Complete other tasks assigned by the leader. Job requirements:
1. Bachelor degree or above in medicine, pharmacy or life sciences;
2. More than 1 year of clinical supervisor or related work experience in pharmaceutical companies or CRO companies; 3. At least 2 or 5 years of clinical research experience, participated in one The supervision of the above registered clinical trials; 4. Experience in clinical research of oncology drugs and products is preferred 5. Familiar with ICH guidelines, GCP and other relevant regulations; 6. Familiar with the whole process of drug development clinical trials 7. Good personal communication skills; 8. Good English, proficient in using computer office software.
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