Clinical Job Opportunity at ICON: Clinical Trial Associate Role in London
Looking for a rewarding clinical job in a global research organization? ICON is hiring a Clinical Trial Associate to support Oncology clinical trials through its Strategic Solutions team. This role offers an excellent opportunity to build a long-term career through ICON careers, gain hands-on clinical research experience, and work in one of the most competitive healthcare jobs markets. With a hybrid setup in Luton, this position is ideal for professionals seeking growth-focused jobs in London.
Job Details:
- Job Position: Clinical Trial Associate
- Company Name: ICON plc
- Job ID: JR143032
- Location: London, United Kingdom, Hybrid Office-Based Role – Luton, England
About the Company:
ICON plc is a world-leading healthcare intelligence and clinical research organization. ICON is known globally for advancing innovation in healthcare jobs and delivering excellence in clinical development. Through ICON careers, the organization fosters an inclusive environment that supports professional growth, collaboration, and diversity. ICON welcomes talented professionals to join its mission to shape the future of clinical research and global healthcare.
Qualifications:
- Bachelor’s degree in a healthcare-related field.
- Prior experience or strong interest in clinical research or similar healthcare jobs.
- Knowledge of clinical trial processes, regulations, and guidelines.
- Excellent organizational and communication skills.
- Ability to work collaboratively in a fast-paced environment with strong attention to detail.
Job Description:
This clinical job is part of the ICON FSP group, working in partnership with one of the world’s leading independent biotechnology companies. ICON is seeking experienced, UK-based Clinical Research Administrators to work in a hybrid home and office-based environment in Luton, England. Candidates should have a solid understanding of clinical trial documentation processes and general CTA responsibilities. This role involves coordination and administration of study activities from start-up through execution and close-out across multiple clinical projects.
Key Responsibilities:
- Assist in the coordination and administration of Oncology clinical trials, ensuring compliance with protocols and regulatory requirements.
- Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.
- Support the preparation of study-related materials such as informed consent forms and case report forms.
- Work with cross-functional teams to facilitate communication and ensure smooth trial execution.
- Contribute to tracking and reporting clinical trial metrics and milestones as part of this clinical job role.
