1.Developing clinical trial protocol and study report.
2.Contribute to the medical/scientific input given for the development of trialrelated documents such as IB, ICF etc. and processes which reside in other line functions.
3.Lead clinical trial data review and generate clinical queries, quality control and data validation for clinical study reports,publications
4.Establish and maintain liaisons with investigators.
5.Serve as back-up medical monitor to provide medical support to trial sites and clinical operation team.
6.Support regulatory filing where medical expertise is required.
1.Graduate from Clinical Medicine with Master degree or above.
2.At least 3-5 year clinical practice / clinical development / clinical research experience. Therapeutic area experience esp solid tumors. Working experience with international pharmaceutical company or CRO is preferable.
3.GCP experience is preferred.
4.Proficiency in English and good computer skill at office software.
5.Excellent planning, organization and problem solving abilities.
6.Good communication and interpersonal skills.