ICON · Reading, UK
The apply link worked recently (not employer-confirmed).
A clinical research organization seeks an experienced Senior CRA to monitor and manage UK-based clinical trial sites, ensuring protocol adherence, regulatory compliance, and data integrity. The role requires minimum 7 years' CRA experience, including 2+ years in oncology studies, and involves frequent site visits, staff training, and cross-functional collaboration with substantial travel requirements.
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.
This role is listed from an approved source. RoleLantern checks that the application link is live and how recently the role appeared — the employer has not confirmed it directly on RoleLantern.
Upload your CV to see which of this role's requirements your background supports, where there may be gaps, and what needs clarification. Private by default — we never sell your CV.
See my match