Prepare data management and statistical analysis sections of project clinical study protocols, summary reports and all study-related documents;
Participate in the development of clinical development strategies for clinical trials, especially in trial design;
Undertake CRF preparation, EDC launching, data entry and other data management work during the implementation of clinical trials;
Conduct statistical analysis of data and prepare reports during the implementation of clinical trials;
Ensure all tests are conducted in strict compliance with the clinical study protocol, company’s SOPs, and national laws and regulations;
Complete other tasks assigned by superiors.
Master's degree or above in biostatistics or other related fields;
Working experience/Industry experience/Position-related experience: Over 3 years of experience in clinical data management or statistical analysis;
Knowledge/Skills: Familiar with medicine-related laws, regulations, GCP and guidelines for clinical trials issued by the Center for Drug Evaluation and Research (CDER); capable of reading, writing and speaking in English; good communication, data collection and analysis capabilities;
Occasional business trips; responsible, clear-headed, organized, self-motivated, proactive, and work well under pressure and in teams.
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
