Clinical Research Coordinator

About the Company The client is a mission-driven organization focused on advancing clinical research through high-quality trial execution and patient-centered care. The team partners closely with Investigators, Sponsors, and CROs to deliver compliant, efficient studies while maintaining the highest standards of research integrity. The environment is fast-paced, collaborative, and rooted in regulatory excellence and continuous improvement. About the Role The client is seeking a Clinical Research Coordinator (CRC) to support the day-to-day coordination and execution of clinical trials. This role is responsible for managing both participant-facing activities and clinical trial data, ensuring all study operations align with protocols, Good Clinical Practice (GCP), FDA regulations, and company SOPs. In this role, you will work closely with Principal Investigators, Sponsors, CROs, and clinical teams to ensure smooth study execution, accurate data collection, and a high-quality patient experience. This is an ideal opportunity for a CRC who thrives in a fast-paced, regulated environment and enjoys balancing clinical responsibilities with data and operational oversight. Key responsibilities include: Coordinate clinical trials under the supervision of the Principal Investigator Ensure compliance with study protocols, GCP, FDA regulations, and SOPs Support participant screening, eligibility review, and informed consent processes Educate participants and families on study procedures and expectations Perform clinical procedures such as vital signs, ECGs, phlebotomy, and specimen processing Maintain accurate source documentation, regulatory files, and study records Enter and manage data in EDC systems, resolve queries, and update CTMS Support recruitment efforts, enrollment tracking, and study startup activities Communicate effectively with Sponsors, CROs, monitors, and internal teams Conduct quality control checks and support audit and compliance activities This role may require flexibility to support multiple clinical sites and adapt to evolving study needs. Requirements Experience & Education Minimum 2 years of experience as a Clinical Research Coordinator or in a related clinical research role At least 1 year of experience in Psychiatry, Neurology, or CNS studies Experience working in GCP and FDA-regulated environments CCRC or CCRP certification preferred Clinical & Technical Skills Experience performing clinical procedures (vital signs, ECG, phlebotomy, specimen handling) Strong understanding of clinical trial processes, protocols, and regulatory requirements Experience with EDC systems, CTMS, and clinical documentation practices Knowledge of medical terminology and clinical practices Core Competencies Strong organizational and multitasking skills in a fast-paced environment Excellent communication and interpersonal skills High attention to detail with strong critical thinking ability Ability to work collaboratively across clinical and operational teams Patient-focused mindset with professionalism and empathy Self-motivated with the ability to manage competing priorities Additional Requirements Ability to work across multiple sites as needed Flexibility to adapt to changing study demands and timelines Commitment to quality, compliance, and research integrity