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Clinical Research Coordinator
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Research Site
Hialeah, FL (In Person)
$57,200 Salary, Full-Time
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Job Description
Clinical Research Coordinator Research Site - 4.0 Hialeah, FL Job Details Full-time $25 - $30 an hour 1 day ago Benefits Health insurance Dental insurance 401(k) Paid time off Vision insurance Life insurance Retirement plan Qualifications HIPAA English Records management Attention to detail Health information management Medical terminology Full Job Description Job Summary We are seeking a dedicated and detail-oriented Clinical Research Coordinator to join our dynamic research team. In this vital role, you will oversee the planning, coordination, and execution of clinical trials to ensure compliance with regulatory standards and study protocols. Your expertise will facilitate accurate data collection, patient monitoring, and documentation review, contributing to groundbreaking medical advancements. This position offers an exciting opportunity to be at the forefront of clinical development while ensuring participant safety and regulatory adherence. Duties Coordinate all aspects of clinical trials, including patient recruitment, screening, enrollment, and follow-up visits Monitor patient progress by recording vital signs, blood sampling, and other clinical assessments in accordance with study protocols Review and verify study documentation for accuracy, completeness, and regulatory compliance Manage data collection and entry using electronic medical record (EMR) systems and adhere to CDISC standards for data management Ensure adherence to FDA regulations, ICH GCP guidelines, and HIPAA privacy rules throughout all trial activities Supervise research staff and collaborate with multidisciplinary teams to maintain high-quality trial conduct Conduct clinical laboratory procedures such as blood sampling and phlebotomy with precision and safety Skills Proven supervising experience in clinical research settings with strong leadership capabilities Extensive knowledge of clinical trials management, including regulatory submissions and compliance management Proficiency in medical terminology, clinical laboratory techniques, and analysis skills for interpreting data Familiarity with statistical software used for data analysis in research environments Understanding of FDA regulations, ICH GCP standards, and CDISC data standards for clinical research Experience with EMR systems, blood sampling procedures, and patient monitoring techniques Strong documentation review skills ensuring accuracy and regulatory compliance in all trial records Join us to make a meaningful impact on healthcare innovation! We are committed to fostering a vibrant work environment that supports your professional growth while advancing critical medical research. This paid position offers an engaging opportunity to develop your expertise in clinical development while working alongside passionate professionals dedicated to improving lives through science.