Job Overview We are seeking a dedicated and detail-oriented Bilingual(Spanish) Clinical Research Coordinator to join our dynamic research team. In this vital role, you will oversee the planning, execution, and management of clinical trials, ensuring compliance with regulatory standards and maintaining high-quality data collection. Your expertise will help advance innovative medical research, improve patient outcomes, and contribute to groundbreaking clinical development efforts. This position offers an exciting opportunity to work at the forefront of healthcare innovation while supporting patient safety and scientific integrity. Responsibilities Coordinate all aspects of clinical trials, including participant recruitment, enrollment, and scheduling. Monitor patient progress throughout study participation, ensuring adherence to protocols and safety guidelines. Review and verify clinical documentation for accuracy, completeness, and regulatory compliance. Collect and manage data using electronic medical record (EMR) systems and adhere to CDISC standards for data consistency. Conduct blood sampling, vital signs measurement, and other clinical procedures such as phlebotomy with precision and care. Ensure compliance with FDA regulations, ICH GCP guidelines, HIPAA privacy rules, and other applicable standards. Supervise research staff and collaborate with multidisciplinary teams to maintain high standards of clinical trial management. Experience Proven supervising experience in a clinical research or healthcare setting. Extensive knowledge of clinical trials management, including patient monitoring and data collection processes. Familiarity with medical terminology, clinical laboratory procedures, and blood sampling techniques. Experience working with EMR systems, statistical software, and adherence to CDISC standards for data management. Certification in Good Clinical Practice (GCP) from a recognized issuer such as ICH or equivalent is required; a valid CA GCP certificate is preferred. Background in nursing or clinical laboratory work is advantageous; strong analysis skills are essential for interpreting study data. Understanding of FDA regulations, HIPAA compliance management, and clinical development processes is necessary for success in this role. Join us to be part of a passionate team committed to advancing healthcare through meticulous research coordination! Minimum 1 Year experience required in similar role.

Experience:

CRC:

1 year (Preferred)

Language:

Spanish (Required)

License/Certification:

drivers license (Required)

Work Location:

In person