Clinical Research Coordinator

Key Responsibilities

• Cover, recruit, and consent eligible patients for research studies.
• Ensure compliance with study protocols, GCP guidelines, and regulatory requirements.
• Collect, document, and maintain accurate study data and source documentation.
• Serve as liaison between investigators, sponsors, CROs, and regulatory bodies.
• Schedule and conduct study visits, including patient education and follow-up.
• Maintain IRB submissions, regulatory binders, and study documentation.
• Auxiliary with monitoring visits, audits, and data queries.

Qualifications

• Minimum 2–3 years of clinical research coordination experience required.
• Experience in rheumatology or autoimmune disease studies strongly preferred.
• Strong understanding of GCP, FDA regulations, and clinical trial processes.
• Excellent organizational, communication, and patient interaction skills.
• Ability to manage multiple studies and deadlines independently.
• Proficiency in EMR systems and clinical trial management software.
• Certification (CCRC, CCRP, or equivalent) preferred but not required.
• Nursing/Clinical background a plus.
• Fluency in Spanish is a plus.

What We Offer

• Competitive salary based on experience.
• Health, dental, and vision insurance.
• Paid time off and holidays.
• Supportive team environment in a reputable private practice.
• Opportunity to contribute to meaningful advancements in rheumatologic care.