Location: Bangalore / Chennai, India (Office-Based or Home-Based)
Company: ICON plc
Job Type: Full-Time
Job ID: JR145001
Experience Required: 8–10 years (Not suitable for freshers)
About the Company
ICON plc is a globally recognized clinical research organization (CRO) delivering healthcare intelligence and innovative clinical development solutions. With a strong presence across global markets, ICON partners with leading pharmaceutical, biotechnology, and medical device companies to accelerate drug development and improve patient outcomes.
Job Overview
The Centralized Clinical Trial Manager (CCTM) plays a strategic role in ensuring the quality, consistency, and compliance of clinical trial operations. This position focuses on centralized monitoring, medical review of site visit reports, and cross-functional coordination to ensure timely issue resolution and adherence to global regulatory standards.
You will act as a critical link between Clinical Research Associates (CRAs), Clinical Trial Managers (CTMs), and Project Managers (PMs), ensuring clinical trial deliverables meet protocol, SOP, and sponsor expectations.
Key Responsibilities
Review site visit reports in accordance with protocol requirements, ICON SOPs, and sponsor guidelines to ensure high-quality documentation
Identify errors, inconsistencies, and risks in clinical trial reports and ensure appropriate escalation
Track and follow up on action items, protocol deviations, and site-related issues for timely resolution
Act as an extension of the CTM team for centralized monitoring, report review, and approvals
Monitor patient safety signals and escalate potential safety concerns identified during report reviews
Ensure consistency and quality across multiple sites and visits, maintaining compliance with timelines and contractual deliverables
Oversee key clinical trial metrics such as monitoring visit reports (MVR), follow-up letters (FUL), and action item closure timelines
Utilize clinical trial systems including CTMS, OMR, and other sponsor/vendor platforms for tracking and reporting
Participate in project meetings, providing insights on quality improvements and operational efficiency
Collaborate with cross-functional teams including Clinical Operations, Data Management, and Pharmacovigilance
Ensure compliance with ICH-GCP guidelines, regulatory requirements, and internal SOPs
Contribute to continuous process improvement initiatives within clinical trial operations
Required Qualifications and Skills
Bachelor’s degree in Life Sciences, Pharmacy, or a related healthcare field (advanced degree preferred)
8–10 years of clinical research experience, including at least 5 years in on-site monitoring
Strong expertise in clinical trial monitoring, centralized monitoring, and clinical data review
In-depth knowledge of ICH-GCP guidelines and global clinical trial regulations
Proficiency in clinical trial systems and data management tools
Excellent analytical, problem-solving, and decision-making abilities
Strong project management and organizational skills
Effective communication and stakeholder management capabilities
Fluency in written and spoken English
Willingness to travel as required
Why Join ICON plc
Opportunity to work on global, high-impact clinical trials
Exposure to advanced clinical trial technologies and centralized monitoring models
Collaborative and inclusive work culture focused on innovation and performance
Strong career growth opportunities within a leading CRO
Compensation and Benefits
ICON offers a competitive compensation package along with comprehensive benefits designed to support employee well-being and long-term career growth, including:
Competitive salary structure
Health insurance coverage for employees and families
Retirement and financial planning benefits
Employee Assistance Programs for mental and emotional well-being
Flexible work arrangements and work-life balance initiatives
Additional country-specific benefits such as childcare support, travel benefits, and wellness programs
Important Note for Applicants
This is a senior-level role requiring significant experience in clinical research and monitoring. Freshers or entry-level candidates are advised to apply for roles such as Clinical Research Associate (CRA), Clinical Trial Assistant (CTA), or Drug Safety Associate before progressing to managerial positions like this.
How to Apply
Candidates interested in advancing their clinical research careers with a global CRO can apply through the official careers portal of ICON plc.
For more verified and regularly updated global job opportunities in Clinical Research, Pharmacovigilance, and Healthcare, visit ThePharmaDaily.com
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