Senior Clinical Research Associate – Contract

ICON plc

Senior Clinical Research Associate at ICON conducting clinical trial monitoring and ensuring compliance with regulations. Working collaboratively with investigators and conducting data analysis for high-quality clinical outcomes.

Posted 4/23/2026contractCalifornia, Kansas, Texas • 🇺🇸 United StatesSeniorWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials
Ensuring protocol compliance, data integrity, and patient safety throughout the trial process
Collaborating with investigators and site staff to facilitate smooth study conduct
Performing data review and resolution of queries to maintain high-quality clinical data
Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Requirements

What you’ll need

Bachelor’s degree in a scientific or health-related field or an equivalent combination of education and clinical research experience
Minimum of 3 years independent monitoring
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
Strong organizational and communication skills, with attention to detail
Ability to work independently and collaboratively in a fast-paced environment
Ability to travel at least 80% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

Benefits

Comp & perks

Paid time off
Remote work options

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

clinical trial processesprotocol compliancedata integritydata reviewquery resolutionstudy documentation preparationclinical study reportsICH-GCP guidelinesindependent monitoring

Soft Skills

organizational skillscommunication skillsattention to detailability to work independentlycollaborative skillsability to work in fast-paced environment