Description

Design and formulate the clinical study protocols and related documents of new drug projects to promote the smooth progress of drug clinical research. Assist in the data management of clinical projects and the review of statistical analysis reports and summary reports. Write clinical study protocols, investigator’s brochures, and other clinically relevant documents. Participate in the planning, initiation, implementation, and management of clinical trials. Cooperate with the research team to ensure the correctness of data in clinical related documents and ensure that medical writing complies with ICH and related regulations.

Requirements

M.Sc. or Ph.D. in Clinical medicine, Biomedicine or other related majors. 3+ years of clinical research work experience, experience in tumor, immune and nervous system drug development is preferred. Familiar with the whole process of clinical research and regulations of clinical trial management regulations. Excellent written and verbal communication skills. Good reading and writing skills in Chinese and English. Good at thinking, strong responsible, good coordination skills and good communication skills.

Director/Manager of Clinical Medical

Description

Requirements

Artivila Therapeutics