Clinical Research Coordinator

Benefits

Job Description

Qualifications

• •Experience Required: 1+ year independently managing clinical studies (Required)
• •Languages: Fluent in English and Spanish (required)
• •Bilingual fluency in English and Spanish (verbal and written)
• •1+ year of experience independently coordinating clinical research studies, including direct responsibility for study visits and regulatory tasks
• •Strong understanding of GCP, human subjects' protection, and clinical research workflows
• •Excellent communication, organizational, and problemsolving skills
• •Ability to work with diverse patient populations and maintain professionalism in sensitive situations
• •Proficiency with EMR systems, eCRFs, and common research platforms (e.g., CTMS tools)

Benefits

• •Health insurance
• •Opportunity for advancement
• •Paid time off
• •Training & development
• •Competitive compensation and benefits
• •Opportunities for professional development and certification
• •A collaborative, missiondriven research environment
• •The chance to contribute to studies that directly impact patient care and health outcomes

Responsibilities

• •Were seeking a Bilingual Clinical Research Coordinator who can independently manage clinical studies from start to finish
• •This role is ideal for someone who has already served as the primary coordinator on their own protocolshandling regulatory tasks, participant coordination, data quality, and study operations with minimal oversight
• •Youll work closely with investigators, sponsors, and participants to ensure studies run smoothly, ethically, and in full compliance with GCP and IRB requirements
• •Serve as the primary coordinator for assigned clinical studies, managing all daytoday operations
• •Conduct participant recruitment, screening, informed consent, and study visits in both English and Spanish
• •Maintain regulatory documentation, including IRB submissions, continuing reviews, amendments, and protocol deviations
• •Coordinate study startup activities, including site initiation, training, and logistics
• •Manage data entry, query resolution, and source documentation to ensure accuracy and audit readiness
• •Communicate with sponsors, CROs, monitors, and internal teams to support study timelines and deliverables
• •Ensure compliance with GCP, FDA regulations, and institutional policies
• •Support budgeting, invoicing, and tracking of studyrelated expenses when applicable