Koreatown/LA, CA- Clinical Research Coordinator

About the role

This Clinical Research Coordinator role supports a nasal polyps clinical trial at a dedicated research site in Koreatown, Los Angeles. You will focus on identifying and recruiting eligible participants, educating them about the study, and helping ensure their continued engagement and compliance throughout the trial. The position calls for strong clinical research experience, excellent organizational skills, and the ability to communicate confidently and professionally with both participants and research staff.

Responsibilities

• Perform patient recruitment activities through targeted community outreach efforts to raise awareness of the nasal polyps clinical trial.
• Partner with local clinics, healthcare providers, and medical professionals to generate patient referrals for the study.
• Educate providers and clinic staff about the clinical trial objectives, eligibility criteria, and participant qualifications.
• Visit local community locations and attend community events to promote the study and identify potential participants.
• Conduct pre-screening of patients to assess eligibility for enrollment in the clinical trial.
• Communicate clearly with potential participants to explain study procedures, expectations, and the importance of adherence.
• Collaborate closely with the research team to support smooth study operations and maintain high standards of participant engagement.
• Maintain accurate documentation related to recruitment, pre-screening, and participant interactions in accordance with regulatory and site requirements.
• Apply clinical research best practices and compliance standards, including HIPAA and GCP, in all aspects of study coordination.

Requirements

• Proven experience working as a Clinical Research Coordinator.
• At least 2 years of experience in patient recruitment for clinical trials.
• Hands-on experience with clinical research and clinical trial processes.
• Strong skills in patient recruitment, including outreach and relationship-building with community and clinical partners.
• Training in HIPAA regulations and patient privacy requirements.
• Training in Good Clinical Practice (GCP) guidelines.
• Excellent verbal and written communication skills for interacting with participants and healthcare professionals.
• Solid organizational skills with strong attention to detail in managing multiple recruitment activities.

Skills

• Experience conducting pre-screening of patients for clinical studies.
• Experience in community outreach or public-facing roles within healthcare or research settings.
• Ability to educate and engage medical providers and community members about clinical research studies.
• Comfort working in a fast-paced research environment with shifting priorities.
• Strong interpersonal skills and the ability to