Clinical Research Coordinator Metropolitan Medical Center - 5.0 Tamarac, FL Job Details Full-time $25 - $30 an hour 1 hour ago Qualifications Statistical software Statistics Data quality checks Microsoft Excel Patient monitoring Electronic health records (EHR) management Data quality assurance

HIPAA ICH

guidelines Documentation tools Supervising experience Records management Team management Attention to detail Data quality monitoring Clinical program monitoring Laboratory compliance Project management experience in healthcare CDISC standards Managing clinical research teams QA/QC Medical record abstraction Health information regulatory compliance Healthcare team management Managing projects Productivity software Research and development project management Managing patient records Clinical data analysis Medical terminology Full Job Description Overview Join our dynamic healthcare research team as a Clinical Research Coordinator, where your expertise will drive the success of vital clinical trials and research projects. This role offers an exciting opportunity to coordinate complex studies, ensure compliance with regulatory standards, and contribute to advancements in medical science. You will play a pivotal part in managing research activities, supporting patient engagement, and maintaining rigorous documentation to uphold the highest quality standards. If you thrive in a fast-paced environment and are passionate about improving patient outcomes through clinical research, this position is perfect for you! Responsibilities Oversee the daily operations of clinical trials, ensuring adherence to study protocols and regulatory guidelines such as FDA regulations and ICH GCP standards. Coordinate patient recruitment, screening, enrollment, and ongoing monitoring to ensure accurate data collection and participant safety. Review and verify clinical documentation, including informed consent forms, case report forms, and medical records, ensuring accuracy and completeness. Manage data entry and data management activities using electronic Medical Record (EMR) systems and adhere to CDISC standards for data consistency. Supervise research staff and collaborate with multidisciplinary teams to facilitate smooth study progression while maintaining compliance with healthcare regulations like HIPAA. Conduct blood sampling, specimen handling, and laboratory procedures in accordance with clinical laboratory standards. Monitor study progress through regular site visits, audits, and quality assurance checks aligned with clinical quality assurance standards. Prepare reports for regulatory submissions, monitor adverse events, and ensure all activities comply with clinical ethical guidelines. Requirements Proven supervising experience in a clinical research or healthcare setting with strong project management skills. In-depth knowledge of medical terminology, clinical research methods, and healthcare compliance requirements such as HIPAA and FDA regulations. Experience reviewing documentation for accuracy and compliance within clinical trials or research projects. Ability to monitor patients effectively during trials, including blood sampling and other clinical procedures. Proficiency in statistical software tools used for data analysis within research contexts. Certification in ICH GCP (Good Clinical Practice) from a recognized issuer; valid certification for CA is preferred. Familiarity with EMR systems, Microsoft Office Suite (Word, Excel, PowerPoint), and data management platforms aligned with CDISC standards. Strong understanding of clinical development processes, research project management, and compliance management practices. Excellent analysis skills combined with meticulous attention to detail to uphold clinical quality assurance standards. Embark on a rewarding career where your dedication enhances the future of healthcare! We are committed to fostering an inclusive environment that supports professional growth while making meaningful contributions to medical science through innovative research efforts.

Pay:

$25.00 - $30.00 per hour Expected hours: 40.0 per week

Work Location:

In person