Senior CRA - Travel-Heavy Global Trials

SupportFinity™

United States

On-site

USD 70,000 - 90,000

Full time

14 days+

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Benefits offered by this job

Various annual leave entitlements

Health insurance offerings

Retirement planning offerings

Global Employee Assistance Programme (

Life assurance

Flexible country-specific benefits

Job summary

ICON plc, a world-leading healthcare intelligence and clinical research organization, seeks a Clinical Research Associate to join our Central/Texas team. You will conduct site visits, ensure protocol compliance, data integrity, and patient safety across trials.

The role requires collaboration with investigators, data review, and study documentation. A Bachelor’s in a scientific/healthcare field, 2+ years as a CRA, ICH-GCP knowledge, and 60% travel readiness are expected.

Qualifications

Bachelor's degree in a scientific or healthcare-related field.
Minimum of 2 years of experience as a Clinical Research Associate.
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
Strong organizational and communication skills, with attention to detail.
Ability to travel at least 60% of the time (international and domestic) and should possess a valid driver’s license

Responsibilities

Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
Collaborate with investigators and site staff to facilitate smooth study conduct.
Perform data review and resolution of queries to maintain high-quality clinical data.
Contribute to the preparation and review of study documentation, including protocols and clinical study reports