临床试验合同专员

1. Draft, review, analyze and negotiate Investigator Site Contracts and budgets, and any other Site related agreements, and escalates to Contract Manager (CM), Clinical Study Manager (CSM) and/or legal as needed;
2. Complete quality check (QC) of final approved contract and budget documents, and initiates signature process of assigned contracts to the responsible signing parties;
3. Ensure final contracts are delivered to agreed timelines, within Fair Market Value & in compliance with relevant legal and regulatory requirements
4. Serve as the primary point of contact between CBO and Global Clinical Operations (GCO), Legal, Investigator Sites and external service providers in accordance with the study related activities to meet business needs;
5. Collect and maintain country and site intelligence information for site, and prepares country/site specific contract process flows as needed;
6. Forecast, set, track and communicate fully executed contract planned dates, and make all efforts to achieve the set planned date, ensuring the CM and study teams are proactively informed of changes and/or risks to the projected dates; each country and/or risks to the projected dates;