Clinical Research Coordinator

About the CompanyThe 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 RoleThe 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 InvestigatorEnsure compliance with study protocols, GCP, FDA regulations, and SOPsSupport participant screening, eligibility review, and informed consent processesEducate participants and families on study procedures and expectationsPerform clinical procedures such as vital signs, ECGs, phlebotomy, and specimen processingMaintain accurate source documentation, regulatory files, and study recordsEnter and manage data in EDC systems, resolve queries, and update CTMSSupport recruitment efforts, enrollment tracking, and study startup activitiesCommunicate effectively with Sponsors, CROs, monitors, and internal teamsConduct quality control checks and support audit and compliance activitiesThis role may require flexibility to support multiple clinical sites and adapt to evolving study needs.RequirementsExperience & EducationMinimum 2 years of experience as a Clinical Research Coordinator or in a related clinical research roleAt least 1 year of experience in Psychiatry, Neurology, or CNS studiesExperience working in GCP and FDA-regulated environmentsCCRC or CCRP certification preferredClinical & Technical SkillsExperience performing clinical procedures (vital signs, ECG, phlebotomy, specimen handling)Strong understanding of clinical trial processes, protocols, and regulatory requirementsExperience with EDC systems, CTMS, and clinical documentation practicesKnowledge of medical terminology and clinical practicesCore CompetenciesStrong organizational and multitasking skills in a fast-paced environmentExcellent communication and interpersonal skillsHigh attention to detail with strong critical thinking abilityAbility to work collaboratively across clinical and operational teamsPatient-focused mindset with professionalism and empathySelf-motivated with the ability to manage competing prioritiesAdditional RequirementsAbility to work across multiple sites as neededFlexibility to adapt to changing study demands and timelinesCommitment to quality, compliance, and research integrity