Job Description:

This role will be onsite in Covina, CA!Responsibilities:Study Coordination:Coordinate and oversee the planning and execution of clinical research studies per protocols and regulatory requirements.Work closely with principal investigators and other study team members to ensure the successful implementation of research projects.Regulatory Compliance:Ensure adherence to regulatory standards and guidelines, including but not limited to FDA regulations, ICHGCP guidelines, and institutional policies.Prepare and submit regulatory documents for study approval and maintain accurate and up-to-date regulatory files.Participant Recruitment and Informed Consent:Recruit and screen eligible participants for clinical trials.Obtain informed consent from study participants and maintain proper documentation.Data Collection and Management:Collect, record, and manage study data accurately and efficiently.Implement data quality control procedures and ensure data integrity throughout the munication and Collaboration:Serve as the primary point of contact for study participants and liaise with interdisciplinary team members, including physicians, nurses, and laboratory municate regularly with sponsors, monitors, and regulatory authorities as needed.Training and Development:Provide training to research staff and ensure ongoing education on study protocols, procedures, and regulatory requirements.Qualifications:Must have prior experience as a Clinical Research Coordinator in a healthcare or research setting (3+ years)Must be Bilingual; Spanish Must be certified in phlebotomy