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Clinical Research Coordinator

Job in Los Angeles, Los Angeles County, California, 90079, USA
Listing for: Amicis Research Center
Full Time position
Listed on 2026-02-22
Job specializations:
  • Research/Development
    Clinical Research, Medical Science, Research Scientist
  • Healthcare
    Clinical Research, Medical Science
Salary/Wage Range or Industry Benchmark: 25 - 45 USD Hourly USD 25.00 45.00 HOUR
Job Description & How to Apply Below

SALARY RANGE : $25-$45/HR DEPENDING ON EXPERIENCE

Company Description

Amicis Research Center is dedicated to excellence in clinical research, guided by the principles of enthusiasm, motivation, and empathy. The organization prioritizes fulfilling research protocol requirements with dedication and fosters a culture of transparency and trust with its research participants. Supported by a skilled team of research assistants, coordinators, nurses, and physicians, Amicis Research Center emphasizes participant well-being while contributing to meaningful advancements in healthcare.

Located in Los Angeles, CA, the center collaborates with CROs and sponsors to drive healthcare innovation.

Role Description

This is a full-time, on-site role for a Clinical Research Coordinator based in Los Angeles, CA. The Clinical Research Coordinator will be responsible for overseeing clinical trials, obtaining informed consent, adhering to research protocols, maintaining thorough documentation, and ensuring compliance with ethical and regulatory standards. Additional responsibilities include coordinating with researchers, study participants, and stakeholders to organize, execute, and monitor clinical trials effectively.

Qualifications
  • Proficiency in managing and obtaining Informed Consent and ensuring ethical compliance in conducting studies
  • Knowledge and experience with research protocols and clinical procedures
  • Hands-on Clinical Research Experience working with clinical data and participants
  • Experience in planning and conducting Clinical Trials
  • Strong organizational and communication skills
  • Proficiency in maintaining accurate and detailed documentation
  • Ability to work collaboratively with a multidisciplinary team
  • Bachelor's degree in a related field or equivalent professional experience in clinical research
  • Certification in Clinical Research Coordination (e.g., ACRP, SOCRA) is a plus
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