Find & Apply For Clinical Research Coordinator Jobs in Edinburg, Texas

Overview Join our dynamic clinical research team as a Clinical Research Coordinator, where you'll play a vital role in advancing healthcare through meticulous management of clinical trials. This position offers an exciting opportunity to oversee study operations, ensure compliance with regulatory standards, and contribute to groundbreaking medical research. You'll coordinate with multidisciplinary teams, monitor patient progress, and uphold the highest standards of data integrity and ethical conduct. If you're passionate about research excellence and thrive in a fast-paced environment, this role is perfect for you to make a meaningful impact on patient care and scientific discovery. Responsibilities Coordinate and oversee all aspects of clinical trial activities, including participant recruitment, enrollment, and follow-up procedures. Ensure adherence to FDA regulations, ICH GCP guidelines, and institutional policies throughout the study lifecycle. Review and verify study documentation for accuracy, completeness, and compliance with regulatory standards. Monitor patient safety by conducting regular assessments, managing adverse event reports, and ensuring proper documentation. Manage data collection processes using EMR (Electronic Medical Record) systems and ensure data quality according to CDISC standards. Supervise research staff and provide training on clinical research methods, ethical guidelines, and compliance management. Collaborate with project teams to develop timelines, track progress, and ensure milestones are met efficiently. Requirements Proven supervising experience in a clinical research or healthcare setting with strong leadership skills. In-depth knowledge of medical terminology, clinical laboratory procedures, and healthcare compliance standards such as HIPAA. Experience reviewing complex documentation including consent forms, case report forms (CRFs), and regulatory submissions. Ability to monitor patients effectively during clinical trials while maintaining strict adherence to ethical guidelines. Proficiency in statistical software tools for data analysis and interpretation of research results. Familiarity with FDA regulations, ICH GCP guidelines, and clinical development processes. Hands-on experience with EMR systems, blood sampling procedures, and clinical trials management platforms. Certification in ICH Good Clinical Practice (GCP) from a recognized issuer is required; valid certification from a CA-approved issuer is preferred for candidates in California. Strong project management skills with experience overseeing multiple research projects simultaneously. Knowledge of CDISC standards for data management and clinical quality assurance standards. Excellent communication skills to facilitate collaboration across multidisciplinary teams while ensuring compliance with clinical ethical guidelines. Embark on a rewarding journey where your expertise will directly influence the future of healthcare!

Pay:

$17.00 - $26.00 per hour Expected hours: 40.0 per week

Work Location:

In person