Conduct literature research for new drug projects;
Develop preclinical pharmacology and toxicology study protocols and plans for ongoing projects;
Design and implement pharmacodynamic tests, pilot toxicology tests and pilot pharmacokinetic tests, perform statistical analysis, and draft reports;
Responsible for the selection, agreement drafting, communication, supervision, coordination and progress follow-up with the commissioned research organizations;
Supervise the study quality of the commissioned organizations and review study data;
Fill in pharmacology and toxicology data in registration application documents;
Provide technical guidance for department personnel.
Master's degree or above in pharmacology, biology or other related fields;
Over 5 years of experience in this position, preferably with independent project management experience;
Competent in management and coordination, learning and innovation, organization and decision-making, pharmacology test operations, and data analysis and compilation;
Attention to detail, strong sense of responsibility, proactive, and ambitious.
If you are interested in this position, please send your resume to us!
Beijing：renshanghe@sumgenbio.com +86-10-56315401-808 Ms. Ren
Hangzhou/Shanghai：hr@sumgenbio.com +86-571-86837379 Ms. Zhao
Copyright Rm. 301, F3, Building C, Block 2, No. 688, Bin'an Road, Changhe Zhejiang ICP Filing No. 18039044
