Clinical Research Coordinator Overview • The Clinical Research Coordinator ensures the execution of clinical studies in compliance with regulatory standards and protocols. • Collaborate with clinical research teams to maintain study integrity and patient confidentiality. • Perform patient screening, consent processes, and follow-up visits to ensure study compliance. • Document patient interactions and study data accurately in electronic systems. • Conduct basic lab procedures, including specimen collection, storage, and shipping. • Maintain effective communication with investigators, sponsors, and team members. • Support study start-up activities, including training and technology setup. • Ensure compliance with HIPAA, GCP, and FDA regulations throughout the study. • Contribute to study recruitment, enrollment, and tracking as required. Clinical Research Coordinator Key Responsibilities & Duties • Screen and enroll patients for clinical studies while ensuring informed consent. • Document and manage patient data in compliance with study protocols. • Perform clinical procedures such as vital signs, ECGs, and phlebotomy. • Coordinate study visits, reminders, and follow-ups for enrolled patients. • Maintain study-specific supplies and ensure proper documentation of adverse events. • Assist with site initiation visits and investigator meetings as needed. • Ensure timely reporting of deviations, adverse events, and compliance issues. • Collaborate with sponsors and IRBs to maintain study integrity. • Support recruitment efforts and maintain positive communication with stakeholders. Clinical Research Coordinator Job Requirements • Bachelor of Science degree with a minimum of 1 year of clinical research experience. • Proficiency in performing clinical procedures such as blood pressure, vitals, and EKGs. • Strong organizational and communication skills with attention to detail. • Experience with electronic health records and data entry systems. • Ability to manage multiple tasks and adapt to changing priorities effectively. • Knowledge of GCP, FDA regulations, and HIPAA compliance standards. • Bi-lingual proficiency in English and Spanish is preferred. • Self-motivated and dependable with a professional demeanor. • Ability to handle sensitive information confidentially and professionally.