Job Overview
We are seeking a highly motivated and detail-oriented Bi-lingual Clinical Research Coordinator to join our dynamic research team. In this pivotal role, you will oversee the day-to-day operations of clinical trials, ensuring compliance with regulatory standards and maintaining the integrity of research data. Your proactive approach will facilitate seamless coordination between investigators, participants, and regulatory bodies, driving forward innovative clinical studies that advance healthcare solutions. This position offers an exciting opportunity to contribute to cutting-edge research in a collaborative and fast-paced environment dedicated to improving patient outcomes.
Duties
- Coordinate all aspects of clinical trial activities, including participant recruitment, scheduling, and follow-up visits
- Review and verify clinical documentation, ensuring accuracy and adherence to protocol requirements
- Monitor patient progress throughout the study, including blood sampling, vital signs, and adverse event reporting
- Manage data collection and entry using electronic medical record (EMR) systems CTMS and EDC systems for data management
- Ensure compliance with FDA regulations, ICH GCP guidelines, HIPAA privacy rules, and clinical ethical standards
- Prepare detailed reports on study progress, deviations, and compliance issues for review by investigators and regulatory agencies
Requirements
- Knowledge of medical terminology, clinical laboratory procedures, and healthcare compliance standards
- Experience reviewing documentation such as consent forms, case report forms (CRFs), and regulatory documents
- Ability to monitor patients effectively while maintaining confidentiality under HIPAA guidelines
- Proficiency in statistical software tools used for data analysis in clinical research environments
- Familiarity with FDA regulations, ICH GCP guidelines, and clinical development processes
- Hands-on experience with EMR systems, blood sampling techniques, and clinical trials management software
- Strong organizational skills with experience managing multiple projects simultaneously within a research setting
- Excellent communication skills for documentation review, team collaboration, and reporting purposes
Join us in advancing medical science through meticulous research coordination! We value dedicated professionals committed to excellence in clinical trials management. This paid position offers an engaging environment where your expertise directly impacts innovative healthcare solutions while supporting your professional growth.
Pay: $24.25 - $26.79 per hour
Benefits:
- Health insurance
- Paid time off
- Vision insurance
Work Location: In person
