Job Profile
Responsible for delivery and/or may manage a team of employees responsible for executing site activation activities that may include:

Site identification and feasibility activities, Regulatory, start-up, and maintenance activities
Preparation, review, negotiation and management of site regulatory documentation and clinical trial agreements with sites and sponsors
Maintains, reviews, and reports on site activation performance metrics
Serves as the primary point of contact for investigative sites and/or sponsors. 
Ensures tracking completion of all regulatory and contractual documents for sites 
Establishes project timelines.
Ensures all site activation activities are performed in accordance with all regulations, SOPs, Work Instructions and project requirements either at the global, regional, or country level and all relevant documents are submitted timely to the Trial Master File as per IQVIA/Sponsor requirements.
Establishes and/or executes goals and objectives for team(s) as well as tracking and delivering on operational/financial performance.
Participates in the broader Global Site Activation planning process; contributes to long-mid range goals and plans; and coordinates activities with other managers and their respective sub-families.

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