北京招聘

职位描述：
1. Prepare and conduct site visits including (but not limited to): qualification visits, initiation visits, monitoring visits, motivational visits, audit support visits, and close-out visits according to relevant SOPs, local requirements, the protocol and project plans as well as providing timely and comprehensive visit and status (i.e. patient recruitment) reports.
2. Communicate effectively with Chiltern Project Team members (i.e. Clinical Team Leader, Project Managers, Safety and Data Management) to ensure study completion per company and client requirements and timelines.
3. Proactively communicate with study sites and follow-up on all open issues in order to meet the project timelines. Ensure that all study-related documentation is tracked, printed, and filed as required by Chiltern SOPs, regulatory requirements, and other protocols.
4. To ensure that investigator site files are assembled appropriately and that all required documentation is in place, tracked and reconciled on a regular basis against the TMF files.
5. May support in mentoring less experienced CRAs on project or department tasks and requirements.
6. Perform other duties as required by the Department or Project Team. 举报 分享

Chiltern is a leading CRO that listens to client needs in order to customize solutions for the Biopharma industry. With a 32 year history, Chiltern delivers globally with therapeutic expertise in oncology, respiratory, anti-infectives / vaccines, ophthalmology and dermatology. Chiltern operates two specialty units: Chiltern Oncology is led by physicians, scientists and clinicians to uniquely manage all phases of hematologic and oncologic clinical drug development; and Chiltern Source is a world leader in tailored relationships for FSP, resourcing and staffing solutions. Chiltern’s 2,200 engaged professionals work across 45 countries to deliver flexible, responsive solutions that are “Designed Around You”.