- Location
- China-Chengdu-Remote
- Workplace
- Remote
- Type
- Full-time
- Department
- Healthcare
- Source
- Workday
Description
When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
Key Role and Responsibilities Summary:
- TMF: Set up and maintain the site level TMF/cTMF, coordinate on document collection, uploading into SharePoint (SP)eTMF, check the document completeness, and provide TMF/eTMF quality control (QC) if required.
- EC Submission: Coordinate on EC submission dossier, site start-up preparation, and EC fee application and tracking.
- Process protocol amendments may include ICF updates.
- Tracker/Metrics Report: Collect and update study trackers/metrics report for site level if needed.
- Site Contract and Payment: Assist in contract signature process; assist in site level payment initiative and payment and invoice tracking.
- Site Materials and Equipment: Distribute site materials and equipment, document printing, shipment, and other administrative work.
- Administrative: Business and department office administration support if required.
- To undertake other reasonably related duties as may be assigned from time to time, as appropriate for level of experience
Skills
Clinical Trials
