上海招聘

职位描述：
1. Document and track study activities using relevant forms and tools, as well as
Chiltern’s Project Management System.
2. Prepare study site files in accordance with relevant SOPs.
3. Create and main contact list of study team members, study sites, and external
suppliers/contract organizations.
4. Minute taking and create documentation for sponsor or internal
teleconferences.
5. Maintain tracking systems for study supplies and investigator payments.
6. Assist in the tracking and filing of documents for all clinical trials into Chiltern’s
global database.
7. Support Investigator Meetings.
8. May support in mentoring less experienced CTAs on project or department
tasks and requirements.
9. Liaise with all other Chiltern departments to ensure the smooth running of the
study.
10. 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”.