職位描述
Responsibilities: Perform all data management activities to ensure the data accuracy and integrity. Manage 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.· 5 years of industry experience in clinical data management will be preferred.· broad knowledge of all stages of data management· Knowledge of ICH GCP and China GCP· Familiar with some sql and SAS programming would be preferred · Willingness and capability to take initiative and support other clinical research units to resolve variety of data management related issues · Mentor or train entry level staff for SAS programming & statistics analysis method· Provide Statistical training for other departments inside organization and coordinate all the effort with other departments to support organization overall goal
