Clinical Research Coordinator

Job Description

Job Description

We are seeking a dedicated and detail-oriented Clinical Research Coordinator (CRC) to join our research team. The CRC will coordinate and manage clinical trial activities for our Rheumatology studies, ensure compliance with regulatory requirements, and support investigators throughout the research process. 

Key Responsibilities: 

• Coordinate and manage day-to-day clinical trial activities. 
• Recruit, screen, and enroll study participants in accordance with protocol guidelines. 
• Obtain informed consent and ensure participant understanding of study requirements. 
• Schedule and conduct study visits, collecting and recording data accurately. 
• Maintain complete and accurate documentation of study activities. 
• Manage regulatory submissions and maintain compliance with GCP, FDA, and IRB guidelines. 
• Facilitate communication between study investigators, sponsors, and study monitors. 
• Assist with monitoring visits, audits, and inspections. 
• Ensure timely reporting of adverse events and protocol deviations. 
• Maintain study supplies and ensure proper specimen handling. 

Qualifications: 

• Bachelor’s degree in a health-related field (e.g., Nursing, Biology, Public Health) required 
• CCRP or CCRC certification preferred 
• Previous experience in clinical or academic research preferred 
• Experience working with diverse populations or in community-based research is an advantage 
• Excellent attention to detail and strong organizational skills 
• Preferably bilingual in English and Spanish (not required) ·