Essential Functions

• Manage assigned opportunities/projects/programs for country or region and adhere to timelines and budget.
• Ensure the site list for assigned studies includes an adequate number of appropriate investigators in accordance with the needs of the sponsor and specifications of the protocol.
• Collect and analyze country/regional Feasibility and/or Site Identification information to meet timelines of each study.
• Attend kick off meetings to understand study requirements include investigator profile, protocol, process specifics and timelines.
• Raise questions and make suggestions based on SID SOPs and Work Instructions.
• Distribute, track, negotiate and review the Confidential Disclosure Agreements (CDAs) for Feasibility and/or Site Identification with input from the study team, management and Legal when appropriate.
• Distribute, track and review Site Questionnaires  for Feasibility and/or Site Information Forms or Site Qualification Questionnaires for SID .
• Ensure completeness, site capability and suitability for the study.
• For SID review SIF and/or SQQ vs the guidance document and approve for SSV or select appropriate sites.
• Manage investigator database entry and quality, ensuring complete investigator and site information is captured and monitor for duplicate entries.
• Maintain and update company information repositories and databases.

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