工作內容：
1. Monitor progress of active clinical research trials and provide communication updates on a regular basis (local and global trials, e.g. US, EU, etc.) 2. Oversee overall integrity of the study and problem-solving skills to promote positive working relationships with the site and staff 3. Manage the training with the clinical teams 4. Responsible for the operational management of clinical studies, ensuring the compliance with timelines, milestones and budget. 5. Oversee site performance, assist with subject eligibility and randomization, identify recruitment problems, help to assure that site keep the recruitment goal on track for trial completion 6. Assist with site feasibility evaluations, identify necessary resources to ensure site performance 7. Act as the main contact to relevant stakeholders and provides input to feasibility, study design, budget development and ensures progress reporting. 8. Provide input on study related documents (e.g. ICF, CRF, monitor plan, protocol, study Procedure Manual etc.), set-up and maintain study files. 9. May stay in foreign country (e.g. Australia) for project tasks such as co-monitoring, site visits, etc. for short-term (within a month). 10. Tasks assigned by the Company
臨床試驗專案(副)經理/專員 (Associate) CPM (Clinical Project Manager) /Project Specialist
我要應徵
