CRA1

Icon

China, ShanghaiFull-time2026-10-27 → 2026-11-10

Core

Coordinate clinical trials, ensure regulatory compliance, and collect/analyze critical data for IVD treatments.

Role type

Clinical Research Associate (CRA)

Builds

Clinical studies for pharmaceutical/IVD sponsors

Domain

Healthcare / Clinical Research / IVD

Required skills

ICH-GCP guidelines knowledge, medical data review, study coordination, stakeholder management, regulatory compliance

Preferred skills

None stated

Technologies

None stated

Responsibilities

Coordinate study setup and monitoring, manage sponsor queries and study costs, prepare feasibility studies, ensure patient safety and regulatory compliance

Seniority

Individual Contributor

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