Clinical Trial Associate
Hybrid · Luton, England, United Kingdom
Job Summary
Coordinate and administer a variety of clinical trials, maintain and organize study documents and regulatory submissions, assist in the preparation of informed consent forms and case report forms, and work with cross-functional teams to ensure smooth trial execution. Track and report clinical trial metrics and milestones. Requires a Bachelor’s degree in a scientific or healthcare-related field, knowledge of clinical trial processes, regulations, and guidelines, excellent organizational and communication skills, and the ability to work collaboratively in a fast-paced environment. The role is UK-based with hybrid home and office-based work in Luton, England, and requires the legal right to work in the country.
Required Qualifications
- Bachelor's degree in a scientific or healthcare-related field
- Prior experience or strong interest in clinical research
- Knowledge of clinical trial processes, regulations, and guidelines
- Excellent organizational and communication skills
- Ability to work collaboratively in a fast-paced environment with attention to detail
- Employment with ICON is contingent upon having the legal right to work in the country where the role is based
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