Job Title: Centralized Clinical Trial Manager
Location: Remote (India – Bangalore, Trivandrum, Chennai)
Company: ICON plc
Employment Type: Full-Time
About the Role:
ICON plc, a global leader in healthcare intelligence and clinical research, is seeking a Centralized Clinical Trial Manager to join our dynamic and diverse team. The role is pivotal in ensuring high-quality, compliant clinical trial monitoring and reporting while supporting trial delivery and patient safety.
Key Responsibilities:
Review and approve visit reports according to annotated reports, study protocols, ICON, and Sponsor SOPs, ensuring accuracy, consistency, and timely turnaround.
Monitor key metrics in OMR, ICOtrial, Sponsor CTMS, and vendor systems, including MVR, FUL timelines, and open action items.
Identify, escalate, and follow up on protocol deviations, outstanding issues, and safety concerns to mitigate risks.
Participate in project meetings to provide feedback on report quality, trends, and process improvements.
Liaise with Clinical Trial Managers (CTMs) and other stakeholders to ensure clinical trial objectives and patient safety are met.
Ensure completion of all necessary trainings to enhance performance, knowledge, and compliance.
Contribute to quality improvement initiatives, risk management plans, and process optimization.
Support change management, staff guidance, and collaboration across teams to improve organizational effectiveness.
Perform other duties as assigned to support clinical operations and trial excellence.
Required Experience & Skills:
6–8 years of onsite clinical monitoring experience, including site monitoring, remote monitoring, and centralized clinical trial management.
Bachelor’s degree in Life Sciences, Healthcare, or related field (advanced degree preferred).
Strong understanding of clinical operations, monitoring activities, and regulatory requirements.
Proficiency in clinical data review, analysis, and interpretation.
Excellent project management, organizational, and multitasking skills.
Effective communication and interpersonal skills to collaborate across diverse teams and functions.
Demonstrated ability to drive process improvements and maintain compliance with SOPs and regulatory guidelines.
Why Join ICON:
Work in a globally recognized organization dedicated to clinical innovation and excellence.
Competitive salary and comprehensive benefits, including health insurance, retirement planning, life assurance, flexible perks, and wellness programs.
Inclusive culture promoting diversity, belonging, and equal opportunity for all employees.
Opportunities for career growth and learning in a supportive and collaborative environment.
Education:
Bachelor’s degree in Life Sciences, Healthcare, or related field (advanced degree preferred).
Core Competencies:
Clinical trial management and monitoring
Centralized and remote monitoring expertise
Data review and interpretation
Stakeholder communication and collaboration
Process improvement and risk management
Team leadership and mentorship
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