上海招聘

Key responsibilities and skills may include, but are not limited to:

Participate in the review of Clinical research documents
Develop Data Management Plan (DMP), maintains DMP throughout lifecycle of study project and ensures DMP is followed according to study design and requirements;
Develop and review Case Report Form (CRF), electronic and/or paper;
Perform external data reconciliation in collaboration with programmers;
Perform training on study trials and create user guides;
Perform database lock/unlock and freeze/unfreeze as appropriate for statistical review, interim review, and or final database lock; Coordinate the archiving of study databases and related documents;
Provide mentorship to junior members;
Working with project manager and cross functional team members to maintain project timeline and overall quality of deliveries.

Requirements

Bachelor’s degree in clinical/pharmacy/biological/mathematical sciences or related field or nursing degree.
At least 2 years data management and/or related work experience in a medical device or pharmaceutical industry/company is preferred.
Working knowledge of Good Clinical Practices, Clinical research, Clinical trial process and related regulatory requirements and terminology.
Working knowledge of Clinical database applications.

成立于2004，泱林是医药研究，医疗器械和化工领域的专业咨询公司。