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. Program PAREXEL Surveys and process investigative site lists in support of site intelligence, feasibility and site selection. Provide operational support for Site Intelligence Data Assets and Systems. Program Parexel Surveys: Provide expertise on survey structure and content to achieve desired results. Process investigative site lists Review site lists to ensure investigator compliance and data completeness. Conduct investigator due diligence... including regulatory, licensure and FCPA checks. Provide expertise on risk associated with compliance issues. Contributes to Sponsor Override process. Monitor change requests. Analyze reports to identify records needing cleaning to maintain data integrity. Support maintenance of data assets Analyze reports to identify records needing cleaning to maintain data integrity. Execute and QC necessary data imports from external and internal systems as needed and verify record change requests. Clean Investigator Database and communicate with Clinical Operations as needed. Review, format and enter Investigator information into Investigator management platform and help raise Service Desk Tickets when issues arise. Maintain appropriate investigator compliance and data protection records. Other Provide training and troubleshooting as well as best practices to internal customers Ensure work adheres to applicable regulatory and legal requirements and Parexel Standard Operating Procedures Maintain a positive, results oriented work environment, building partnerships and modeling teamwork, communicating to the team in an open, balanced and objective manner Headquartered near Boston, Massachusetts and in Durham, North Carolina, Parexel has over 16,000 employees, with offices that support clients in over 100 countries around the world. We provide the most comprehensive drug development capabilities of any CRO worldwide. Our global regulatory expertise, Phase I-IV clinical research services, and advanced commercialization services all work together to move you through the development journey more smoothly and cost-effectively from beginning to end
Taiwan

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