Senior Clinical Research Associate

United States of AmericaRemoteFull-time2026-10-07 → 2026-11-11

Core

Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials to ensure protocol compliance, data integrity, and patient safety.

Role type

Senior Clinical Research Associate (IC)

Builds

Clinical trial data and study documentation

Domain

Healthcare / Clinical Research

Required skills

Clinical trial monitoring, Protocol compliance, Data integrity management, ICH-GCP guidelines knowledge, Site qualification, Query resolution, Study documentation preparation

Preferred skills

Independent monitoring experience, International travel capability, Valid driver's license

Technologies

Clinical trial management systems, Electronic data capture (EDC)

Responsibilities

Conduct site qualification, initiation, monitoring, and close-out visits; Ensure protocol compliance and data integrity; Collaborate with investigators and site staff; Perform data review and resolve queries; Prepare and review study documentation including protocols and clinical study reports

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