上海招聘

职位描述：
? Identification of potential investigational sites
? Coordinates and performs comprehensive site management
? Conduct of pre?study, initiation, interim and close out monitoring visits
? Produces comprehensive visit reports and status reports
? Resolves data issues and audit issues
? Adherence to the study timelines and budget
? Mentors less experienced CRAs
? Within International (when applicable)? collects high quality essential documents and supports completion of ethics committee and
regulatory submissions in association with the respective departments in Theorem Clinical Research.
? Completes all other assignments given by management or as business needs require.
? Within Europe – when applicable, the collection of high quality essential documents and completion of ethics committee and regulatory
- submissions in association with Clinical Services Centre

Requirements:
- 3-4 clinical trial experience in global CRO or Pharm. Medical device experience preferred. 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”.