Clinical Research Associate

A-Line Staffing Solutions

Irvine, CAFull-time and ContractorPosted Apr 13, 2026

Behavioral Health Market Context

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Benefits

Dental CoverageHealth Insurance

Job Description

 Work: Play a key role in conducting clinical trials that are at the forefront of healthcare. Your contributions will ensure that trials are compliant with regulatory standards and that data integrity is maintained.
• Collaborative Environment: You will be a vital part of a cross-functional team, working alongside some of the brightest minds in the industry. Build lasting connections with site personnel, researchers, and key stakeholders.
• Professional Growth: With opportunities for continuous learning and development, you’ll be encouraged to propose solutions that streamline processes and improve efficiency.

Your Role Includes:
• Driving the success of clinical trials by supporting and coordinating study startup activities.
• Performing thorough remote monitoring visits and generating comprehensive reports.
• Cultivating strong relationships with site personnel and internal partners to enhance site enrollment and performance.
• Assisting with site remediation activities to uphold the highest standards of quality.

Qualifications We’re Seeking:
• Education: Bachelor’s Degree or Equivalent in Life Sciences or Nursing is a must!
• Experience: Bring 3-4 years of clinical research experience (either as a CRC or CRA), with a solid understanding of quality assurance/control and regulatory compliance.
• Skills: Familiarity with electronic data capture is preferred. A clinical research certification (ACRP or SoCRA) is a bonus!

Perks of Joining Us:
• Enjoy a comprehensive benefits package after just 90 days of employment.
• Get ready for a secure future with our 401(k) plan featuring company match after 1 year of service.
• Be part of an AI-driven organization that enhances human decision-making and fosters innovation!

If you’re a proactive individual looking to make a significant impact in clinical research, we want to hear from you!

INDKL

Pay: $60.00 per hour

Benefits:
• 401(k)
• Dental insurance
• Health insurance
• Vision insurance

Work Location: In person

Qualifications

  • Education: Bachelor’s Degree or Equivalent in Life Sciences or Nursing is a must!
  • Experience: Bring 3-4 years of clinical research experience (either as a CRC or CRA), with a solid understanding of quality assurance/control and regulatory compliance
  • A clinical research certification (ACRP or SoCRA) is a bonus!

Benefits

  • Impactful Work: Play a key role in conducting clinical trials that are at the forefront of healthcare
  • Enjoy a comprehensive benefits package after just 90 days of employment
  • Get ready for a secure future with our 401(k) plan featuring company match after 1 year of service
  • Pay: $60.00 per hour
  • 401(k)
  • Dental insurance
  • Health insurance
  • Vision insurance

Responsibilities

  • Your contributions will ensure that trials are compliant with regulatory standards and that data integrity is maintained
  • Collaborative Environment: You will be a vital part of a cross-functional team, working alongside some of the brightest minds in the industry
  • Build lasting connections with site personnel, researchers, and key stakeholders
  • Professional Growth: With opportunities for continuous learning and development, you’ll be encouraged to propose solutions that streamline processes and improve efficiency
  • Driving the success of clinical trials by supporting and coordinating study startup activities
  • Performing thorough remote monitoring visits and generating comprehensive reports
  • Cultivating strong relationships with site personnel and internal partners to enhance site enrollment and performance
  • Assisting with site remediation activities to uphold the highest standards of quality


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