Description

1. Responsible for formulating clinical development strategies for new drugs; 2. Fully responsible for the formulation of clinical trial plans for new drugs and the writing, review, and revision of medical related documents; 3. Responsible for the overall management and technical control of medical review, medical supervision, medical analysis, and medical support during clinical trials; 4. Communicate and coordinate with external medical experts and review experts to ensure project execution; 5. Conduct medical research, analysis, and information support for the determination of new projects; 6. Responsible for the department management and operation of the Medical Department, including the development and review of work plans, work standards and processes, personnel organization and management, and the development of departmental performance evaluation plans and supervision of execution.

Requirements

1. Integrity, high sense of responsibility and team spirit, strong communication and coordination skills; 2. Doctoral degree in clinical medicine, pharmacology, oncology, and related fields; At least three years of clinical medical experience in pharmaceutical companies or CRO for new drugs; 3. Familiar with clinical trial management processes, familiar with GCP, ICH-GCP, drug registration regulations, and various pharmaceutical policies; 4. Strong ability to search Chinese and English literature and medical information, as well as write reports.

Medical Director

Description

Requirements

RegeneCore Biotech