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Hybrid Clinical Research Associate Job at ICON plc UK
Are you looking for a rewarding Clinical Research Associate role within a global CRO? This exciting position at ICON plc offers dynamic Hybrid Jobs in Reading, United Kingdom, combining remote flexibility with on-site monitoring excellence. If you are exploring jobs in UK clinical research or seeking a strong job opportunity for life science graduates, this role within ICON plc Careers provides international exposure, career growth, and competitive benefits.
About the Company
ICON plc is a world-leading healthcare intelligence and clinical research organization headquartered in Dublin. With operations worldwide, ICON supports pharmaceutical, biotechnology, and medical device companies across all phases of clinical development. Through ICON plc Careers, the organization promotes diversity, innovation, and high performance. Employees benefit from competitive compensation, comprehensive health insurance options, retirement planning, life assurance, flexible benefits, and access to the Global Employee Assistance Programme, LifeWorks. ICON fosters a culture where clinical professionals thrive in Hybrid Jobs that balance performance and well-being.
Job Details
- Job Title: Clinical Research Associate I / II (Sponsor Dedicated)
- Company: ICON plc
- Location: Reading, United Kingdom
- Department: Clinical Monitoring – Full Service & Corporate Support
- Work Model: Remote or Office-Based
- Job Reference: JR145397
About the Clinical Research Associate Role
ICON plc is seeking a Clinical Research Associate (CRA I or CRA II level) to join its research team in a sponsor-dedicated capacity. This position plays a key role in overseeing and coordinating clinical trials, ensuring regulatory compliance, and collecting and analyzing essential study data.
The role is dedicated to one of ICON’s valued sponsors and requires independent monitoring and strong stakeholder collaboration.
Key Responsibilities
- Independently coordinate all activities related to study setup and monitoring
- Complete accurate study status reports and maintain comprehensive study documentation
- Manage sponsor-generated queries efficiently
- Take responsibility for study cost efficiency
- Participate in the preparation and review of study documentation and feasibility assessments for new proposals
- Develop and maintain strong working relationships with key stakeholders, clinical investigators, and site staff
- Ensure patient safety through compliance with ICON procedures, study protocols, and regulatory requirements
Candidate Profile
- University degree in Science/Life Sciences
- Minimum of 12 months of independent on-site monitoring experience within a CRO or pharmaceutical company
- Strong knowledge of ICH-GCP guidelines and the ability to review and evaluate medical data
- Excellent written and verbal communication skills in English
- Strong interpersonal skills and the ability to respond to queries in a timely manner
- Ability to travel domestically across the UK (via car and air travel) and possession of a valid driver’s license
Compensation & Benefits Of Clinical Research Associate
ICON offers a competitive salary and a comprehensive benefits package designed to support employee well-being and work-life balance. Benefits may include:
- Annual leave entitlements
- Health insurance options
- Retirement planning programs
- Global Employee Assistance Programme (LifeWorks) with 24-hour access to specialized professionals
- Life assurance
- Flexible country-specific optional benefits, such as childcare vouchers, bike purchase schemes, gym membership discounts, subsidized travel passes, and health assessments.
