Job 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.
Responsibilities
TMF: Set up and maintain the site level TMF/cTMF, coordinate on document collection, uploading into SharePoint (SPVeTMF, 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 IF 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
Qualifications
Bachelor's degree or above in life sciences, English, and/or management.
0.5 years of clinical trial experience in the pharmaceutical or CRO industry. Exceptions may be considered based on level of training and mentoring available.
Read, write, and speak fluent English; fluent in host country language may be required.
Excellent organizational skills and ability to prioritize and multitask.