Clinical Research Coordinator Jobs in Florida

Job Summary

We are seeking a dynamic and detail-oriented Clinical Research Coordinator to join our innovative research team. In this vital role, you will oversee the planning, execution, and management of clinical trials, ensuring compliance with regulatory standards and ethical guidelines. Your expertise will facilitate the smooth operation of research projects, from participant recruitment to data collection and analysis, contributing to groundbreaking advancements in healthcare. This position offers an exciting opportunity to work in a fast-paced environment dedicated to improving patient outcomes through high-quality clinical research.

Responsibilities

• Coordinate all aspects of clinical trials, including participant recruitment, screening, enrollment, and follow-up assessments.
• Ensure adherence to FDA regulations, ICH GCP guidelines, HIPAA privacy standards, and clinical ethical protocols throughout all phases of research.
• Review and verify clinical documentation for accuracy, completeness, and compliance with study protocols.
• Monitor patient safety by conducting regular assessments and managing adverse event reporting in accordance with regulatory requirements.
• Manage data collection and entry using electronic medical record (EMR) systems and comply with CDISC standards for data management.
• Supervise research staff and collaborate with multidisciplinary teams to maintain project timelines and quality assurance standards.
• Prepare reports for regulatory submissions, audits, and institutional review boards (IRBs), ensuring all documentation aligns with clinical development objectives.
• Utilize statistical software for data analysis to support research findings and contribute to scientific publications or presentations.

Qualifications

• Proven supervising experience in a clinical or healthcare setting with strong leadership skills.
• Comprehensive knowledge of medical terminology, clinical research methods, and healthcare compliance regulations such as FDA guidelines and HIPAA.
• Experience reviewing clinical documentation and managing data within EMR systems; familiarity with CDISC standards is a plus.
• Demonstrated ability to monitor patients effectively during clinical trials, including blood sampling and other procedures requiring clinical laboratory experience.
• Proficiency in Microsoft Office suite (Word, Excel, PowerPoint) for report writing and project management; experience with statistical software is highly desirable.
• Certification in ICH GCP (Good Clinical Practice) from a recognized issuer; valid certification for CA or equivalent is preferred.
• Strong understanding of clinical quality assurance standards, research project management, and compliance management within a research setting.
• Excellent analysis skills coupled with meticulous attention to detail to ensure high-quality data collection and reporting.
• Ability to work efficiently in a fast-paced environment while maintaining strict adherence to ethical guidelines and regulatory requirements.

Join us in advancing healthcare through meticulous research coordination! We are committed to fostering an inclusive environment where your expertise can make a meaningful impact on patient care worldwide. All roles are paid positions dedicated to supporting your professional growth within the vibrant field of clinical research.

Pay: $20.00 - $27.00 per hour

Work Location: In person