CRA - Multi Sponsor

Madrid💼 Full-time🗓 2025-07-11 → 2026-08-04

Core

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

Role type

Senior Clinical Research Associate (CRA)

Builds

Clinical trials for healthcare and life sciences clients

Domain

Clinical research / Healthcare intelligence

Deliverable

client delivery

Required skills

Clinical trial process management, regulatory compliance, site monitoring, data integrity management, project management, clinical trial software proficiency

Preferred skills

Advanced degree in life sciences, nursing, or medicine, experience managing multiple sites and projects simultaneously, training and guidance of site staff

Technologies

Clinical trial software and tools

Responsibilities

Monitoring clinical trial sites for protocol and GCP 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