Oncology Clinical Research Associate - Travel Focus

ICON

Austin (TX)

On-site

USD 70,000 - 95,000

Full time

14 days+
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Benefits offered by this job

Annual leave
Health insurance
Retirement plan
LifeWorks EAP
Life insurance

Job summary

ICON Strategic Solutions, part of ICON, is seeking a Clinical Research Associate in the Women's Oncology space for the West/Central/South region. You will monitor trials, ensure patient safety and data integrity, and collaborate with investigators to enable compliant study conduct.

The role requires 2+ years in CRA roles with oncology experience, travel up to 50%, and strong knowledge of ICH-GCP. ICON offers a sponsor-dedicated model, global expertise, and competitive benefits.

Qualifications

  • Bachelor's degree in a scientific or healthcare-related field.
  • Minimum of 2 years of experience as a Clinical Research Associate.
  • Oncology monitoring experience required.
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
  • Willingness to travel up to 50% within region (West, Central or South).

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.

Skills

Oncology monitoring
Clinical trial monitoring
Data review
Regulatory knowledge
Travel readiness

Education

Bachelor's degree in science/healthcare

Job description

ICON Strategic Solutions, part of ICON, is seeking a Clinical Research Associate in the Women's Oncology space for the West/Central/South region. You will monitor trials, ensure patient safety and data integrity, and collaborate with investigators to enable compliant study conduct.

The role requires 2+ years in CRA roles with oncology experience, travel up to 50%, and strong knowledge of ICH-GCP. ICON offers a sponsor-dedicated model, global expertise, and competitive benefits.

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