Job Summary We are seeking a dedicated and energetic Clinical Research Coordinator/Research Nurse to join our dynamic research team. In this role, you will be instrumental in managing and executing clinical trials, ensuring adherence to regulatory standards, and providing exceptional patient care throughout the research process. Your expertise will help advance innovative medical treatments and contribute to the development of new therapies, making a meaningful impact on patient outcomes and scientific progress. This position offers an exciting opportunity for healthcare professionals passionate about research, clinical development, and compliance to thrive in a collaborative environment committed to excellence. Duties Coordinate all aspects of clinical trials, including participant recruitment, enrollment, and follow-up, ensuring compliance with study protocols and regulatory guidelines. Monitor patient safety by conducting regular assessments of vital signs, blood sampling, and overall health status while documenting findings accurately in electronic medical records (EMR) systems. Review and verify documentation such as consent forms, case report forms (CRFs), and source documents to maintain data integrity and regulatory compliance. Oversee clinical laboratory procedures, including phlebotomy and blood sample collection, adhering to safety standards and laboratory protocols. Manage data collection, entry, and management using statistical software and adhere to data management standards such as CDISC (Clinical Data Interchange Standards Consortium). Ensure compliance with FDA regulations, ICH GCP guidelines (International Conference on Harmonisation Good Clinical Practice), HIPAA privacy rules, and healthcare compliance standards. Supervise research staff and coordinate project timelines, budgets, and deliverables to ensure smooth project progression while maintaining high-quality standards in clinical trials. Skills Proven supervising experience in clinical research or healthcare settings with strong leadership capabilities. Extensive knowledge of medical terminology, clinical research methods, and ethical guidelines governing human subject research. Proficiency in documentation review, data management systems, EMR platforms, and statistical software used for analysis. Familiarity with FDA regulations, ICH GCP certification (or equivalent), and clinical trial management practices. Experience with clinical laboratory procedures such as phlebotomy, blood sampling, vital signs measurement, and analysis skills. Strong project management skills with the ability to coordinate multiple tasks within strict timelines while ensuring compliance with clinical quality assurance standards. Excellent communication skills for effective collaboration with multidisciplinary teams including clinicians, regulatory bodies, and study participants. Knowledge of CDISC standards for data collection and reporting; proficiency in Microsoft Office Suite for documentation purposes. Join us to be part of a forward-thinking organization where your expertise will directly contribute to groundbreaking medical research! We value your commitment to excellence in clinical development while supporting your professional growth in a vibrant research environment dedicated to improving lives through science.

Pay:

$30.00 - $45.00 per hour

Work Location:

In person