CRA

UK, Reading💼 Full-time🗓 2026-07-06 → 2026-09-29

Core

Overseeing and managing clinical trial activities to ensure adherence to protocols, regulatory requirements, and GCP standards while ensuring data integrity and participant safety.

Role type

Senior Clinical Research Associate (CRA)

Builds

Clinical trials for new medicines and treatments

Domain

Healthcare / Clinical Research

Required skills

Clinical trial monitoring, site management, data integrity, regulatory compliance (GCP), clinical trial software proficiency, travel management

Preferred skills

Advanced degree in life sciences, nursing, or medicine, experience managing multiple sites and projects simultaneously

Responsibilities

Monitoring clinical trial sites for protocol and regulatory adherence, conducting site visits to assess performance and resolve issues, collaborating with cross-functional teams for data collection, providing training to site staff and CRAs, building relationships with site personnel and stakeholders

Seniority

Senior, hands-on IC

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About Icon

ICON is seeking a Project Engineer to support our Design-Build team. The Project Engineer will play a key role in ensuring seamless coordination between design and construction activities, serving as the primary liaison between ICON's design, engineering, and field operations teams during construction. This role requires exceptional attention to detail, strong technical and communication skills, and the ability to manage information flow with speed, precision, and accountability. As a core member of the Project Management Office (PMO), the Project Engineer supports the Project Executive and Pr

CRA