Clinical Research Associate II — Site Monitoring & Data Integrity

KCR Placement

Texas

On-site

USD 70,000 - 95,000

Full time

14 days+

A complete application in a minute

Tailored resume and cover letter, ready to send.

Get past ATS filters

Benefits offered by this job

Annual leave entitlements

Health insurance offerings

Retirement planning offerings

Employee assistance program

Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate II to support sponsor-dedicated monitoring in the Midwest. You will design and analyze trials, interpret complex data, and contribute to advancing therapies for patients worldwide.

You will conduct site visits, ensure data integrity, and collaborate with investigators to drive study success while traveling about 60% of the time. A scientific/healthcare background and strong organizational skills are essential.

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 work independently and collaboratively in a fast-paced environment.
Willingness to travel as required (approximately 60%).

Responsibilities

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