Senior Clinical Research Associate

Czech Republic, Prague, CZ🌐 Remote💼 Full-time🗓 2026-08-25 → 2026-10-07

Core

Oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and GCP standards.

Role type

Senior Clinical Research Associate (CRA)

Builds

Clinical trial execution and data integrity

Domain

Healthcare / Clinical Research (via careerplan.io/jobs/JR158746-senior-clinical-research-associate-at-icon)

Deliverable

physical/clinical work

Required skills

Clinical trial monitoring, site management, data integrity, regulatory compliance, GCP standards, clinical trial software proficiency

Preferred skills

Independent work, guiding others, managing multiple sites/projects, problem-solving, influencing compliance

Responsibilities

Monitor clinical trial sites for protocol and regulatory adherence, conduct site visits to assess performance and resolve issues, collaborate on data collection and reporting, provide training to site staff and CRAs, build relationships with site personnel and stakeholders

Seniority

Senior, hands-on IC

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