Role Overview
ICON is hiring a entry-level Clinical Research Associate Focused on Trial Management and Data Integrity. This is a full-time role in CA. posted last week. Full responsibilities, required qualifications, and the apply link are listed in the description below.
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Job Description
Play a major role in conducting successful clinical trials as a Clinical Research Associate. Ensure compliance with study protocols and maintain data integrity through proactive site management. This pivotal position requires managing clinical trial activities effectively while ensuring all operations meet regulatory standards and Good Clinical Practice (GCP).
You will utilize your advanced degree and extensive CRA experience to oversee various sites, conduct performance assessments, and collaborate with diverse teams for accurate reporting and participant safety. Key Responsibilities:
- Monitor trial sites for regulatory compliance
- Conduct site visits to address and solve issues
- Collaborate on data collection and reporting
- Train site staff to uphold trial conduct standards
- Cultivate relationships with site stakeholders Requirements:
- Advanced degree in life sciences, nursing, or medicine required
- Significant experience as a Clinical Research Associate
- Strong organizational and problem-solving capabilities
- Knowledgeable in relevant clinical trial software
- Excellent communication and relationship-building skills Utilize your skills in compliance and monitoring to influence the success of clinical trials while contributing to the advancement of healthcare innovation.
Frequently Asked Questions
How do I apply for the Clinical Research Associate Focused on Trial Management and Data Integrity position at ICON?
Use the Apply button above to submit your application directly to ICON. Most applications take less than 5 minutes if your resume and contact details are ready, and you'll be routed to the employer's official application system to finish.
Where is the Clinical Research Associate Focused on Trial Management and Data Integrity position at ICON located?
This position is based in CA. ICON has not indicated remote or hybrid options for this role, so candidates should plan for on-site work.
What does a Clinical Research Associate Focused on Trial Management and Data Integrity at ICON earn?
ICON has not disclosed a salary range in this posting. Many employers share specifics later in the interview process; you can also ask during a recruiter screen if compensation transparency is important to you.
When was the Clinical Research Associate Focused on Trial Management and Data Integrity role at ICON posted?
This role was posted on May 28, 2026 (11 days ago). It's still listed as actively hiring; we re-confirm openings against the source system multiple times per day and remove closed roles.
Is the Clinical Research Associate Focused on Trial Management and Data Integrity role at ICON entry-level?
Yes. This is an entry-level position. Strong candidates typically have 0-2 years of relevant work experience, internships, or significant project work. Read the full description for any specific qualification requirements ICON has listed.
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