Job Title: Centralized Clinical Trial Manager
Location: Bangalore / Home-Based, India
Job ID: JR135179
Job Type: Full-Time
Category: Clinical Trial Management / Clinical Operations
ICON plc is a world-leading healthcare intelligence and clinical research organization, committed to advancing clinical development through innovation and excellence. We foster a collaborative and inclusive environment, empowering employees to deliver high-quality clinical research and data-driven insights globally.
Join ICON to play a pivotal role in clinical trial management and help shape the future of healthcare.
We are seeking a Centralized Clinical Trial Manager to oversee centralized monitoring activities across clinical trials. In this role, you will ensure data-driven insights enhance trial quality, regulatory compliance, and patient safety. You will collaborate with cross-functional teams to ensure timely, accurate, and efficient study execution while supporting continuous process improvement.
Uphold and promote ICON’s values, emphasizing commitment to people, clients, and performance.
Create and maintain a culture of process improvement to streamline trial activities and meet client needs.
Review and approve visit reports, ensuring consistency, accuracy, and adherence to protocol, SOPs, and sponsor standards.
Oversee study metrics using OMR, ICOtrial, CTMS, and vendor systems to ensure timelines, action items, and quality metrics are achieved.
Identify, escalate, and follow-up on open action items, protocol deviations, and safety concerns.
Attend project meetings and provide feedback for continuous improvement in trial quality and report consistency.
Collaborate with other managers to optimize operational efficiency and effectiveness.
Support staff in change management and provide training to improve performance.
Contribute to quality improvement and risk management plans, minimizing impact on project objectives and patient safety.
Perform additional duties as assigned.
Domestic and/or international travel may be required (~5%).
Proven experience in clinical trial management or centralized monitoring in clinical research.
Strong knowledge of clinical trial processes, SOPs, and regulatory guidelines (ICH-GCP, sponsor standards).
Demonstrated ability to manage timelines, prioritize tasks, and escalate risks effectively.
Excellent written and verbal communication skills with strong attention to detail.
Leadership and collaboration skills to work with cross-functional teams and support process improvement initiatives.
Work on global clinical trials and gain exposure to modern centralized monitoring technologies and data-driven solutions.
Competitive salary and comprehensive benefits including health insurance, retirement plans, life assurance, and flexible work options.
Supportive and inclusive work environment emphasizing professional development and continuous learning.
Contribute directly to patient safety and quality clinical research outcomes globally.
Apply Now: Submit your CV/resume via the ICON careers portal or application link.
Equal Opportunity Employer: ICON is committed to inclusion, diversity, and providing reasonable accommodations for qualified candidates.
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