Clinical Research Coordinator

Company Description

3Sync Research has been dedicated to serving patients' needs since its establishment in 2021. The company focuses on enhancing patient lives by delivering high-quality services in clinical trials. With a commitment to compliance and a strong emphasis on compassionate care, 3Sync Research strives to set a standard of excellence in clinical research. The organization is grounded in the belief that ethical and empathetic practices lead to better outcomes for patients and advancements in healthcare.

Role Description

This is a contract, on-site role for a Clinical Research Coordinator located in Los Angeles, CA. The Clinical Research Coordinator will manage clinical trials, oversee research processes, and ensure compliance with relevant protocols. Responsibilities include obtaining informed consent from participants, managing research documentation, maintaining accurate and organized records, and ensuring adherence to clinical trial protocols. The coordinator will play a vital role in ensuring ethical and efficient execution of research projects with a patient-centered approach.

Qualifications

• Experience with Informed Consent processes and a thorough understanding of participant rights and confidentiality
• Comprehensive knowledge and experience with Protocols and Clinical Trials
• Proven track record of Clinical Research Experience and conducting research studies
• Strong organizational, communication, and problem-solving skills
• Detail-oriented with the ability to manage multiple tasks and deadlines
• Bachelor’s degree in a related field; additional certifications in clinical research are a plus
• Familiarity with regulatory guidelines for clinical research is preferred