Responsibilities: 1) Administrative support; 2) Desk research to summarize some basic information of clinical trial related; 3) Coordinate with regional team on the China registered site information; 4) Maintain and update teams request tracker, external medical advisor list, internal study experience tracker, etc; 5) Work closely with legal team about the latest version of ICA(Contract), and document stamp/signature support; 6) Work closely with finance team on the payment application and status tracking. Requirements: Bachelor's Degree and above, Life sciences or other related field Skilled in use of Microsoft Office (especially MS Excel skills, Python is a plus); Knowledge of clinical trial; Strong written and verbal communication skills including good command of English language; IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. EEO Minorities/Females/Protected Veterans/Disabled