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3.0 - 7.0 years
0 Lacs
karnataka
On-site
As a Centralized Clinical Trial Manager at ICON, you will be responsible for leading the centralized monitoring activities for clinical trials to ensure trial quality and patient safety. Your key responsibilities will include: - Leading the centralized monitoring activities for clinical trials, including data review and risk-based monitoring. - Collaborating with clinical operations, data management, and biostatistics teams to identify potential risks and ensure proactive management of trial data. - Ensuring study compliance with regulatory requirements and protocols by overseeing real-time data reviews and monitoring activities. - Providing oversight on site performance, patient safety, and...
Posted 1 month ago
2.0 - 4.0 years
0 Lacs
hyderabad, telangana, india
On-site
The Data Surveillance Analyst (DSA) is responsible for analyzing scientific and operational data to support the Data Surveillance process and reviewing project-specific Quality Tolerance Limits. They assist in developing Data Surveillance Plans (DSPs) and conduct defined project reviews. The DSA also attends internal and external Data Surveillance meetings, where they present relevant findings to the project team. Key Accountabilities Data Surveillance Plan Development and Technology Configuration: Support the development of a robust Data Surveillance Plan, including Key Risk Indicators, Quality Tolerance Limits, and central statistical analysis Configure and Maintain Data Surveillance techn...
Posted 1 month ago
0.0 years
0 Lacs
bengaluru, karnataka, india
On-site
Centralized Clinical Trial Manager, Bangalore/Home-based ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Centralized Clinical Trial Manager to join our diverse and dynamic team. As a Centralized Clinical Trial Manager at ICON, you will play a crucial role in overseeing the centralized monitoring activities of clinical trials, ensuring the smooth coordination of data-driven insights to enhance trial quality and patient safety. You will contribute to the advan...
Posted 2 months ago
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