Responsibilities:

- Select, manage, and serve as the primary point of contact with CRO, vendors and study sites.
- Monitor the quality of CRO/vendor deliverables.
- Support study document development such as protocol, IB and ICF etc.

- Support site management and fully involved in resolving study related issues. - Support KOL management.
- Study timeline/budget management and clinical trial agreement negotiation. - Ensure that study milestones and budget are met as plan.

- Smooth cross-functional communication internally and support overall development of clinical studies.（If SPM，need take lead role of internal cross function communication）and evaluate risk and benefit, drive decision made between team and stakeholder
- Host project meetings, discussions and deliver meeting minutes, track all follow up actions to be done.
- Project related tasks assigned by line manager such as internal process optimization, communication pathway optimization, organize non-project training for clinical development etc.  

Requirements:

1.2 years above project management experience, preferably handle study independently. SPM will require 4 years above project management experience.

2.Excellent English-speaking skills is preferably

3.Great communication skill and strong self-motivation to drive things happen.

4.Teamwork spirit and ownerships.