Descripción del trabajo
IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients.
Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.
Provides operational support to the Clinical Research organization to ensure the successful and timely start-up of sites in the region.
This includes actions related to Site ID up to site ready to enrol. Performs regulatory and ethics submissions, negotiate contracts with the sites, collect essential documents all in accordance with regulations, SOPs, and project requirements either at the global, regional, or country level.
Primary point of contact for investigative sites; tracks completion of regulatory and contractual documents for sites; and establishes project timelines.