Senior Clinical Trial Assistant (Senior CTA) – Clinical Trial Support
Location: Blue Bell
Job Reference: JR144532
Company: ICON plc
Division: ICON Strategic Solutions
Department: Clinical Trial Support
Work Model: Remote
Job Overview
ICON Strategic Solutions is seeking a highly organized and experienced Senior Clinical Trial Assistant (Senior CTA) to support global clinical trial operations. This role is critical in ensuring accurate documentation management, regulatory compliance, and seamless coordination across study teams.
The Senior CTA will provide operational and administrative support across the clinical trial lifecycle, working closely with Clinical Research Associates, Project Managers, investigators, and sponsors to ensure timely and compliant study execution.
This opportunity is ideal for clinical trial support professionals seeking career advancement within a global CRO environment.
Key Responsibilities
Provide comprehensive administrative and operational support for clinical trials
Maintain and manage essential trial documentation within eTMF and CTMS systems
Assist in preparing, reviewing, and submitting regulatory documents in accordance with ICH-GCP and regulatory requirements
Coordinate meetings, track action items, and support cross-functional communication
Monitor study progress, timelines, and key milestones
Manage site communications and ensure timely distribution of study materials
Support audit and inspection readiness through accurate documentation control
Build strong working relationships with site staff and internal stakeholders
Proactively identify operational issues and support resolution efforts
Required Experience
Minimum 5–7 years of experience in clinical trial support or Clinical Trial Assistant roles within a pharmaceutical company or CRO
Strong understanding of clinical trial processes, documentation standards, and regulatory compliance requirements
Hands-on experience with CTMS, eTMF, EDC, and other clinical systems
Experience supporting multi-site or global clinical trials preferred
Educational Qualifications
Bachelor’s degree in Life Sciences, Healthcare, Clinical Research, or a related field preferred
Relevant clinical research certifications are advantageous
Core Competencies
Strong knowledge of ICH-GCP guidelines and regulatory documentation standards
Exceptional organizational and multitasking abilities
High attention to detail and data accuracy
Effective communication and stakeholder coordination skills
Ability to manage competing priorities in a fast-paced clinical research environment
Proactive problem-solving mindset
Why Join ICON plc?
ICON plc is a leading global clinical research organization delivering outsourced drug development and commercialization services to pharmaceutical, biotechnology, and medical device companies worldwide. ICON supports clinical programs across all phases, ensuring operational excellence and regulatory compliance.
Employees benefit from:
Competitive compensation and performance-driven rewards
Comprehensive health insurance options
Retirement savings and financial planning programs
Generous annual leave entitlements
Global Employee Assistance Programme (LifeWorks)
Life assurance coverage
Flexible, country-specific employee benefits
ICON is committed to fostering an inclusive and diverse workplace, offering equal employment opportunities and long-term career growth within the clinical research industry.
Apply now through ThePharmaDaily.com to advance your career in clinical trial support with a globally recognized clinical research organization.
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