Clinical Trial Manager (CTM) – Clinical Operations & Study Leadership
Location: Bangalore, India (Role aligned with Mumbai operations)
Job Type: Full-Time | Office-Based (Non-Flex)
Company: ICON plc
Job ID: JR144479
About the Role
ICON plc, a global leader in healthcare intelligence and clinical research, is seeking an experienced Clinical Trial Manager (CTM) to lead end-to-end clinical trial execution. This role requires strong expertise in clinical operations, project management, and cross-functional coordination to ensure successful delivery of clinical studies within defined timelines and quality standards.
As a key contributor, you will manage local trial operations, collaborate with global stakeholders, and ensure compliance with regulatory requirements while maintaining high-quality clinical trial performance.
Key Responsibilities
Lead and manage clinical trial activities in compliance with study protocols, ICH-GCP, and SOPs
Oversee site selection, site initiation, monitoring, and close-out processes
Act as the primary interface between investigators, site teams, vendors, and global study teams
Ensure timely achievement of study milestones while proactively managing risks and resolving issues
Drive quality oversight, site performance metrics, and monitoring excellence
Support regulatory inspections and audits, ensuring continuous inspection readiness
Provide guidance and oversight to Clinical Research Associates (CRAs)
Ensure effective cross-functional collaboration across clinical operations teams
Required Qualifications & Experience
Bachelor’s degree in Life Sciences, Pharmacy, or a related field
Minimum 12+ years of experience in Clinical Operations with strong onsite monitoring background
At least 2–3 years of clinical project management or study leadership experience
Strong knowledge of ICH-GCP guidelines and global regulatory requirements
Proven experience in Oncology, Cardiology, or Pulmonology clinical trials
Demonstrated ability to manage complex clinical studies under tight timelines
Excellent stakeholder management, communication, and problem-solving skills
Ability to perform effectively in high-pressure, fast-paced environments
Preferred Skills
Experience managing multi-site or global clinical trials
Strong leadership and decision-making capabilities
Exposure to risk-based monitoring and performance metrics
Why Join ICON
ICON offers a dynamic and performance-driven environment where clinical operations professionals can lead impactful studies and contribute to advancing global healthcare innovation.
Key Benefits Include
Competitive salary and career growth opportunities
Structured, office-based work environment
Generous leave policies
Comprehensive health insurance coverage
Retirement and financial planning benefits
Global Employee Assistance Programme (24/7 support)
Life insurance and wellness initiatives
Flexible, country-specific employee benefits
Diversity, Equity & Inclusion
ICON is committed to creating an inclusive workplace. All qualified applicants will receive equal opportunity without discrimination.
Application Note
Candidates who may not meet every requirement are encouraged to apply. ICON values diverse experience and supports continuous career development.
This role is ideal for senior clinical operations professionals looking to lead trial execution, manage complex studies, and drive operational excellence within a leading global CRO.
Uttar Pradesh :
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Frank Scottile Blvd |Missouri :
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Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
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China | Quarry Bay |Liaoning :
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Netherlands |Remote Australia :
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England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |North Yorkshire :
Harrogate |South Yorkshire :
Sheffield |Oxfordshire :
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Zaventem |South America :
Peru | Argentina |Brazil :
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Tartu | Estonia |Harju County (Maakond) :
Tallinn |Hà Nội :
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