Trial Delivery Manager – Advanced | Clinical Project Management
Location: Blue Bell
Job Reference: JR144444
Company: ICON plc
Division: ICON Strategic Solutions
Department: Clinical Project Management
Work Model: Remote
Job Overview
ICON Strategic Solutions is seeking an experienced Trial Delivery Manager (Advanced) to lead global clinical trial delivery within a dynamic and highly regulated research environment. This senior-level role is responsible for overseeing end-to-end clinical project execution, ensuring trials are delivered on time, within scope, and in compliance with regulatory and sponsor requirements.
The Trial Delivery Manager will drive operational excellence, manage cross-functional clinical teams, and ensure alignment with strategic objectives across complex pharmaceutical and biotechnology development programs.
This position is ideal for experienced clinical project leaders with strong therapeutic knowledge and a proven track record in global trial management.
Key Responsibilities
Develop and execute comprehensive clinical trial delivery plans aligned with sponsor objectives
Lead cross-functional teams including Clinical Operations, Regulatory Affairs, Data Management, and Safety
Oversee project timelines, budgets, risks, and quality metrics to ensure successful trial execution
Define project scope and deliverables in collaboration with stakeholders and sponsors
Monitor trial progress and proactively mitigate operational risks
Ensure compliance with ICH-GCP, FDA, EMA, and other applicable regulatory standards
Drive inspection readiness and audit preparedness across assigned studies
Prepare and present project reports, metrics, and performance updates to senior leadership and sponsors
Mentor and guide team members, fostering continuous improvement and high-performance culture
Integrate industry best practices and emerging technologies into clinical project strategies
Required Experience
Minimum 8–12 years of progressive experience in clinical research, including substantial experience in clinical project or trial management
Proven track record of leading global or multi-regional clinical trials within pharmaceutical or biotechnology organizations
Demonstrated expertise in managing complex study timelines, budgets, and vendor oversight
Strong knowledge of ICH-GCP, global regulatory frameworks, and clinical development processes
Experience working within a CRO environment preferred
Educational Qualifications
Bachelor’s degree in Life Sciences, Pharmacy, Business Administration, or a related field required
Master’s degree in Project Management, Clinical Research, or Business Administration preferred
Core Competencies
Advanced clinical trial management and strategic planning expertise
Strong leadership and team development capabilities
Excellent analytical and risk management skills
Proficiency in clinical project management systems and tools
Exceptional stakeholder communication and presentation skills
Ability to manage multiple global projects in a fast-paced environment
Why Join ICON plc?
ICON plc is a world-leading clinical research organization delivering outsourced development solutions to pharmaceutical, biotechnology, and medical device companies globally. With a strong reputation in healthcare intelligence and operational excellence, ICON supports the full clinical development lifecycle from early-phase trials to post-marketing studies.
Employees benefit from:
Competitive compensation structure
Comprehensive health insurance options
Retirement and long-term savings programs
Generous annual leave policies
Global Employee Assistance Programme (LifeWorks)
Life assurance coverage
Flexible, country-specific employee benefits
ICON is committed to fostering an inclusive workplace that promotes innovation, diversity, and professional growth.
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