Clinical Research Job at ICON plc UK
Looking for a clinical research job in the UK with global impact? ICON plc is hiring a CRC Level 1 in London, offering an excellent job opportunity for life science graduates eager to build hands-on experience in clinical trials. This role is ideal for candidates aspiring to grow as a clinical research coordinator while working with one of the world’s leading clinical research organizations. If you are exploring a job in UK clinical research with long-term career growth, this opportunity at ICON stands out.
About ICON plc
ICON plc is a global leader in clinical research and healthcare intelligence, partnering with pharmaceutical, biotechnology, and medical device companies worldwide. Through ICON plc careers, professionals contribute to transforming clinical development and improving patient outcomes across the globe.
Job Details:
- Job Title: CRC Level 1
- Location: London, United Kingdom (Office-based – South London, Orpington)
- Job Reference: JR138729
- Business Area: ICON Full Service & Corporate Support – Clinical Research Site Services
- Work Model: Office Based
About the Clinical Research Job Role
ICON is seeking a CRC Level 1 to join its diverse and dynamic team in London. In this role, the Clinical Research Coordinator will support the coordination and execution of clinical trial activities while contributing to the advancement of innovative treatments and therapies through high-quality clinical research.
Key Responsibilities
- Assist in the coordination and implementation of clinical trial activities under the guidance of Clinical Research Coordinators, including patient recruitment, screening, and enrollment
- Support the maintenance and organization of study documentation and regulatory files in compliance with protocols and regulatory standards
- Collect, record, and enter study data into databases and electronic data capture (EDC) systems in accordance with study protocols and SOPs
- Assist with the preparation and submission of regulatory documents and correspondence to regulatory authorities and Institutional Review Boards (IRBs)
- Provide logistical support for study visits, meetings, and research-related activities, including scheduling appointments, arranging travel, and coordinating study materials
Candidate Profile
- Bachelor’s degree in life sciences, or a related field; relevant experience may be considered in lieu of a degree
- Previous experience in a clinical research or healthcare setting is preferred but not required
- Strong organizational skills and attention to detail, with the ability to manage multiple tasks and priorities effectively
- Excellent communication and interpersonal skills with the ability to interact professionally with study participants and colleagues
- Proficiency in Microsoft Office applications (Word, Excel, Outlook) and willingness to learn new software tools
What ICON Can Offer in a Clinical Research Job?
ICON places strong emphasis on its people and has built a diverse culture that rewards high performance and nurtures talent.
Benefits include:
- Competitive salary
- Various annual leave entitlements
- A range of health insurance options for employees and their families
- Competitive retirement planning offerings
- Global Employee Assistance Programme (LifeWorks) with 24/7 access to a network of specialized professionals
- Life assurance
- Flexible, country-specific benefits such as childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, and health assessments
