Main Tasks:$- Lead clinical data management work in clnical trials as trial Data Manager.$- Review & comment on protocols, especially with focus on standardization of data collection, use of Case Report Form standard modules.$- Supervise the set-up of CRF to ensure that contents, composition and design confirm with the respective protocol, the project standard and all applicable SOPs.$- Co-ordinate the set-up, formatting, sending and receipt of electronic data with laboratories (CDP trials).$- Create annotation, trial validation plan and trial deriviation plan.$- Perform query management and DCFs generation and tracking.$- Generate trial documentation such as Data handling protocol/Report and Raw Data Listings, organize database release meeting.$- Prepare related documentations for statistical analysis and clinical trial report.$- Contribute to reports including clinical reports in the form of listings based on raw data in collaboration with trial members.$- Provide feedback on trial data quality to trial team$- Organize, plan and schedule his/her own participation in projects.Plan, co-ordinate, supervise and evaluate the DM activities for local clinical trials and CDP trials.$- Bring to the attention of the DM alternative/additional tools, facilities, methods, techniques.$- Contribute to generation of a co-operation and collegial atmosphere within the trial team and department.$- Perform Data coding with WhoDrug and MedDRA dictionary in TMS system.$$Qualifications:$- Bachelors degree is required, preferably in medical related field.$- In-depth knowledge of the data management process.$- Computer proficiency required; familiar with SQL language, Programming skills of database software, i.e.Oracle, SAS, or Access required.$- Comprehensive knowledge of the structure of database.$- Excellent spoken and written English.$- 2-3 years working experience in Data management work, preferable in the field of relation database system.