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Job Overview
Join our dynamic team as a Clinical Research Coordinator and become a vital driver in advancing healthcare through innovative clinical trials. In this role, you will oversee the planning, execution, and management of clinical research projects, ensuring adherence to regulatory standards and ethical guidelines. Your energetic approach will help streamline study operations, monitor patient safety, and maintain meticulous documentation to support groundbreaking medical discoveries. This paid position offers an exciting opportunity to work within a collaborative research environment dedicated to improving patient outcomes worldwide.
Responsibilities
- Coordinate all aspects of clinical trial activities, including participant recruitment, enrollment, and retention.
- Review and verify study documentation for accuracy, completeness, and compliance with FDA regulations and ICH GCP standards.
- Monitor patient progress throughout the trial, including blood sampling, data collection, and adverse event reporting.
- Manage study timelines, budgets, and resource allocation to ensure project milestones are met efficiently.
- Supervise research staff and collaborate with multidisciplinary teams to uphold clinical quality assurance standards.
- Ensure compliance with healthcare regulations such as HIPAA and clinical ethical guidelines during all research activities.
- Utilize electronic medical records (EMR) systems and data management software to accurately document trial data in accordance with CDISC standards.
Skills
- Proven supervising experience in a clinical or research setting with strong leadership capabilities.
- Extensive knowledge of medical terminology, clinical development processes, and research project management.
- Proficiency in statistical software and data analysis tools relevant to clinical trials.
- Familiarity with FDA regulations, ICH GCP guidelines, and healthcare compliance standards such as HIPAA.
- Experience with clinical laboratory procedures including blood sampling and sample processing.
- Strong documentation review skills coupled with meticulous attention to detail for data collection and regulatory compliance.
- Competence in using Microsoft Office Suite (Word, Excel, PowerPoint) for report writing and project coordination.
- Certification in Good Clinical Practice (GCP) from a recognized issuer for CA or equivalent is highly desirable.
- Ability to manage multiple projects simultaneously while maintaining high standards of quality assurance.
- Excellent communication skills to effectively liaise with research teams, regulatory bodies, and study participants.
This role is perfect for proactive professionals eager to make an impact in the field of clinical research by ensuring rigorous study conduct while fostering innovation in healthcare solutions. Join us to be part of a forward-thinking organization committed to scientific excellence and ethical integrity!
Pay: $20.00 - $27.00 per hour
Work Location: In person
