As Clinical Project Manager, You will:
1. Fully understanding the project protocol and implementation of clinical trials, discuss and execute task items with project team members and clinical site staff.
2. Support clinical project management and the development/implementation of training programs.
3. Participate in the project initiation meeting, the summing-up meeting and other clinical trial stage meetings.
4. Monthly work summary and project progress management to ensure the project is carried out according to the overall plan.
5. Process clinical data independently, from project initiation to database locking.
6. Accomplish other project-related tasks and duties as requested by management.
Qualifications:
1. Bachelor's degree or above in medicine, pharmacy, biotechnology or related major.
2. 2~5 years project management experience in IRC focused on Oncology.
3. Good command of computer and Microsoft Office.
4. Excellence in communication skill.
5. English as the working language, experience of overseas study is preferred.