Join Ruining
Medical Manager
Job Responsibilities:
1. Responsible for the writing and review of medical materials related to innovative drugs, including clinical reviews, clinical trial protocols, informed consent forms, investigator manuals, clinical summary reports and other medical materials, data statistics related materials and drug vigilance related materials review, etc.;
2. Responsible for the medical support of innovative drug clinical trials, including medical monitoring, data analysis and the writing and review of relevant materials in the clinical trial process;
3. Responsible for the collection, collation and analysis of medical strategy related materials in the development process
of innovative drugs; 4. Responsible for the daily medical-related internal and external communication and coordination of innovative drug projects; including communication and coordination with principal investigators, clinical medicine experts, review experts, etc. according to the needs of clinical projects.
Job Requirements:
1. Clinical medicine-related majors, master's degree or above;
2. More than 2 years of pre-marketing medical affairs work experience or more than 5 years of clinical doctor work experience;
3. Understand the innovative drug development process and related requirements, drug registration and clinical trial medical related processes and requirements;
4. Familiar with the design of clinical trial protocols and the writing of related materials and medical support work in clinical trials;
5. Good English skills, with literature retrieval and reading and writing skills.