Apply for Centralized Clinical Trial Manager job at ICON plc India. Check eligibility, responsibilities, salary, and clinical research career opportunities now.
Introduction
The Centralized Clinical Trial Manager Job at ICON plc is a senior-level opportunity for experienced clinical research professionals. This role focuses on centralized monitoring, quality review of clinical trial data, and coordination between global study teams. If you have strong experience in clinical operations and monitoring, this position offers excellent career growth, global exposure, and flexible working options.
Job Overview
| Job Details | Information |
|---|---|
| Job Title | Centralized Clinical Trial Manager |
| Company Name | ICON plc |
| Location | Bangalore / Chennai (Remote or Office) |
| Employment Type | Full-Time |
| Department | Clinical Operations / Clinical Trials |
| Experience Required | 8–10 Years |
| Education | Bachelor’s Degree (Advanced Preferred) |
| Salary | As per company norms |
Company Overview
ICON plc is a leading global healthcare intelligence and clinical research organization providing outsourced development and commercialization services to pharmaceutical, biotechnology, and medical device companies. With a strong focus on innovation and patient-centric research, ICON supports the development of life-saving therapies across the globe.
Job Location & Employment Type
- Locations: Bangalore / Chennai, India
- Work Mode: Office-based or Home-based (Hybrid flexibility)
- Employment Type: Full-Time
Open Positions / Department Details
This role is part of the Clinical Trial Management team, where professionals focus on centralized monitoring, data review, and ensuring compliance with clinical trial protocols and SOPs. The position acts as a bridge between CRAs (Clinical Research Associates), CTMs (Clinical Trial Managers), and Project Managers.
Key Roles & Responsibilities
The Centralized Clinical Trial Manager Job at ICON plc involves high-level responsibilities in clinical trial monitoring and coordination:
Clinical Trial Monitoring & Oversight
- Review site visit reports to ensure compliance with protocols and SOPs
- Maintain high-quality standards in clinical trial documentation
- Identify and escalate issues, errors, and safety concerns
Coordination & Communication
- Act as a liaison between CRA, CTM, and Project Manager
- Ensure timely resolution of action items and protocol deviations
- Communicate trends, risks, and study updates to stakeholders
Quality & Compliance Management
- Ensure consistency and accuracy across visit reports
- Monitor key clinical metrics such as timelines and action items
- Ensure adherence to ICH-GCP guidelines and regulatory requirements
Data Review & Risk Management
- Analyze clinical trial data for trends and potential risks
- Identify safety signals and escalate appropriately
- Support continuous improvement of trial processes
Project & Process Improvement
- Participate in project meetings and provide improvement suggestions
- Support process optimization and efficiency enhancements
- Ensure timely completion of reports as per contractual timelines
Eligibility Criteria
Education
- Bachelor’s degree in Life Sciences, Healthcare, or related field
- Advanced degree preferred
Experience
- 8–10 years of experience in clinical research
- Minimum 5 years of on-site monitoring experience
- Experience in clinical trial management and centralized monitoring
Skills Required
- Strong knowledge of clinical trial processes and ICH-GCP guidelines
- Expertise in data review and clinical report analysis
- Excellent project management and organizational skills
- Strong communication and stakeholder coordination abilities
- Ability to manage multiple studies and deadlines
- Proficiency in clinical systems (CTMS, trial platforms)
- Problem-solving and analytical thinking skills
- Flexibility to travel if required
Salary & Benefits
- Salary: As per company norms
- Additional benefits include:
- Health insurance plans for employees and families
- Paid annual leave and work-life balance programs
- Retirement and financial planning benefits
- Employee assistance programs for mental well-being
- Flexible work arrangements (remote/hybrid)
- Career development and training opportunities
Selection Process
The hiring process typically includes:
- Resume shortlisting
- HR discussion
- Technical/functional interview
- Final interview and offer
How to Apply
Interested candidates can apply for the Centralized Clinical Trial Manager Job at ICON plc through the official online application portal. Ensure your resume highlights clinical trial monitoring experience and leadership skills.
Important Dates
- Application Deadline: Apply as soon as possible
Why Apply for This Job?
Here’s why this role is highly valuable:
- Work with a globally recognized clinical research organization
- Gain exposure to advanced clinical trial monitoring techniques
- Opportunity to lead and manage multiple clinical studies
- Flexible work options (remote or office-based)
- Strong career growth in clinical operations and trial management
- Competitive salary and comprehensive benefits
This position is ideal for experienced professionals aiming to move into leadership roles in clinical research.
FAQs
1. What does a Centralized Clinical Trial Manager do?
This role focuses on reviewing clinical trial data, managing reports, and ensuring compliance with protocols and regulations.
2. What experience is required for this job?
Candidates need 8–10 years of clinical research experience with strong monitoring expertise.
3. Is this a remote job?
Yes, it offers both remote and office-based working options.
4. What skills are essential for this role?
Key skills include clinical data analysis, project management, communication, and regulatory knowledge.
5. How can I apply for this job?
You can apply through ICON plc’s official online careers portal.
Conclusion
The Centralized Clinical Trial Manager Job at ICON plc 2026 is a premium opportunity for experienced clinical research professionals. With leadership responsibilities, global exposure, and flexible working options, this role offers excellent career progression in clinical trial management. Apply now to take your career to the next level.
Disclaimer
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