Study Start Up Associate I - India, Bangalore Hybrid: Office based

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive setting driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.

Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.

That’s our vision. We’re driven by it. And we need talented people who share it.
If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive setting,



with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.

Job Responsibilities:
Review of site level essential documents ensuring that Sponsor and Investigator obligations are being met and are in compliance with ICON SOPs/WIs, Sponsor SOPs, applicable country requirements and ICH/GCP guidelines.
Update systems in a timely and accurate way, maintaining site-related data in applicable clinical systems according to procedures and guidelines.
Preparation and Submission of Investigational Product Release Pack.
Ensure accuracy and timely completeness of Trial Master File (TMF) documents by submitting the documents for filing to TMF during start-up.
Perform timely and accurate task progress communication.
Be highly organized in an workplace with shifting priorities.
Interact successfully with internal stakeholders.
Performs all tasks in accord

📌 Study Start Up Associate I Bengaluru
🏢 Icon
📍 Bengaluru