Clinical Trial Assistant (FSP) Wuhan

When our values align theres no limit to what we can achieve.

At Parexel we all share the same goal - to improve the worlds 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 were 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