職位描述
Responsibilities: Perform all data management activities to ensure the data accuracy and integrity. Support the progress of the project and prioritizes with respect to pre-determined timelines. Work with project teams to ensure smooth transmissions of data. The detail data management activities include but not limit to:· Design Data Management Plan and report the data progress periodically.· Database design and CRF design and annotation.· CRF review and CRF completion guidelines.· Data validation Plan development and data validation checks programming.· SAS programming of listings.· Generation and tracking of data clarifications form.· Updating the database and database quality control.· Blind data review and database lock.· File archiving for all of the data management documents.· All other duties as assigned. Qualifications: · College or above education in medical, public health, pharmacology, or other related fields.· 1 years of industry experience in clinical data management will be preferred.· Vast knowledge of all stages of data management· Knowledge of ICH GCP and China GCP· Familiar with sql and SAS programming is preferred · Fluent in written and sporken English with CET 6· Excellent computer and communication skills· Willingness and capability to take initiative and help Clinical Research and Statisticians resolve data problems· Be able to work independently and complete a high volume of work
