临床前项目主管 - 恒瑞-全球精英计划
3 weeks ago
Location: Shanghai Role and Responsibilities:
1. Responsible for the preclinical development (including pharmacodynamics, pharmacokinetics and safety) of their respective projects (priority in oncology, immunology, hematology, etc.) as required by the line manager.
2. Responsible for the audit and quality assurance of the undertaking unit of the corresponding project;
3. Be responsible for the progress of the corresponding project and effectively promote the project;
4. Responsible for the preparation, improvement and upgrading of relevant SOP of the Preclinical Pharmacology and Toxicology Department.
Qualification Requirements:
1. Education requirement: doctoral degree or above, overseas background is preferred.
2. Major requirements: major in pharmacology (tumor, immunology, metabolism, cardiovascular, etc.), toxicology, molecular biology and cell biology.
3. Working experience: 0 ~ 3 years working experience in the industry.
4. Capability requirements:
1) Have strong leadership and execution capabilities;
2) Have rich experience in management and coordination;
3) Have the ability to express clearly in writing and verbally, and be good at active and active communication;
4) They possess the ability to work independently but also possess a strong sense of collectivity and a strong spirit of teamwork. Yes
5) Have excellent problem-solving ability and emergency plan management ability.
5. Skill requirements:
1) Extensive knowledge and management experience in the pharmaceutical industry;
2) Be familiar with Drug Administration Law, New Drug Approval Measures, GLP, ICH, etc., and understand the whole process of drug preclinical research;
3) Have skills in training and presenting at investigator meetings;
4) The ability to independently consult relevant literature and write various reports.
6. Foreign language requirements: proficiency in English.
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