Preparation of study trackers and updates to the sponsors
Assist with preparation of study documentation under the guidance of the Project Manager.
Liaise with external vendor to obtain translation of site/ patient documents, including initial quotes
Assist with managing access requests to Connected Devices applications and databases
Conduct biannual access review for Connected Devices applications and databases
Create and maintain the Trial Master File. Assist with periodic review of study files for accuracy and completeness.
Assist with uploading project documentation on Connected Devices logistic systems
Coordinate with Logistics team for site creation/updating and other deliverables
Assist with the project archival tasks
May perform assigned administrative tasks to support team members with project
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. Learn more at
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