Experienced Bilingual Clinical Research Coordinator (Spanish/English)

Company Description Accurate Clinical Research, Inc. is a dedicated clinical research organization focused on conducting high-quality clinical trials that support the development of safe and effective therapies. The company partners with sponsors and investigators to ensure studies are carried out with integrity, regulatory compliance, and strong participant protections. Team members collaborate across disciplines to deliver accurate data and positive participant experiences. The organization values professionalism, clear communication, and consistent attention to detail in all aspects of research operations.Role Description This is a full-time, on-site Experienced Bilingual Clinical Research Coordinator (Spanish/English) role based in Baytown, TX. The coordinator will manage day-to-day study activities, including screening and enrolling participants, explaining and obtaining informed consent in both Spanish and English, and scheduling study visits. Responsibilities include maintaining source documents and case report forms, ensuring protocol adherence, coordinating with investigators and sponsors, and overseeing regulatory and regulatory binders. The coordinator will handle data entry, query resolution, and sample collection logistics, while monitoring participant safety, reporting adverse events, and ensuring compliance with Good Clinical Practice (GCP) and site SOPs. The role also involves serving as a primary point of contact for participants, providing clear communication, and supporting retention throughout each clinical trial.QualificationsStrong experience with informed consent processes, including explaining study procedures and risks clearly in both Spanish and English.Proficiency in protocol interpretation and implementation, ensuring strict adherence to study guidelines and visit schedules.Demonstrated clinical research experience, including coordination of study visits, data collection, and regulatory documentation.Hands-on experience working with clinical trials, including subject recruitment, eligibility assessment, and ongoing participant follow-up.Fluency in Spanish and English, with excellent written and verbal communication skills in both languages.Knowledge of GCP, ICH guidelines, and relevant FDA or regulatory requirements for human subjects research.Strong organizational, time-management, and problem-solving skills, with the ability to manage multiple studies simultaneously.Comfort working directly with diverse participant populations in an on-site clinical setting.Proficiency with electronic data capture systems, EMR/EHR platforms, and standard office software.Previous experience as a Clinical Research Coordinator or similar role in a site, hospital, or research center setting strongly preferred and/or Current certification in clinical research (e.g., ACRP, SOCRA) is a plus.