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IQVIA, a leading global provider of clinical research services and healthcare insights, is seeking to support regionally-based clinical studies in execution from initiation through closeout. The role covers all study activities in line with SOPs, aiming to meet quality and timeline metrics while coordinating with sponsors and internal teams.
Responsibilities include vendor management, tracking timelines and budgets, producing reports for management, and assisting in budget approval and invoice
Oncology experience a plus but not required. Assist in the execution of the assigned regionally-based clinical study(ies) per Contract, from initiation through to closeout. Support all clinical study related activities for assigned projects in accordance with SOPs, policies and practices, meeting quality and timeline metrics.
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 committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.