1.Job Purpose
1.1 This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical study studies in accordance with Tigermed or sponsor Standard Operating Procedures (SOPs), International Conference on Harmonization Good Clinical Practice standard (ICH-GCP), Clinical Practice standard (GCP) and other applicable regulations.
1.2 The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget.
2.Responsibilities
(a) Site management
(b) Drug Safety
(c) Finance and Administration
(d) Study Tools and system
3. Qualifications:
3.1 Bachelor degree or above in Medical, Pharmacology or Biology related major. The excellent candidates will not be restricted to the current requirements;
3.2 At least 3 year of CRA experience;
3.3 Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/procedures;
3.4 Good skills on Microsoft Word, Excel, PPT and Outlook, etc.
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