Research Coordinator

Benefits 401(k) 401(k) matching Dental insurance Health insurance Paid time off Vision insurance Research Coordinator – Clinical Trials Rehabilitation & Neurological Services, LLC is seeking an experienced, organized, dependable, and motivated Clinical Research Coordinator to join our growing clinical research team. We are looking for a reliable professional who wants to grow with our organization long-term and become an integral part of a fast-paced, patient-centered research program. This position requires someone who can work independently, prioritize responsibilities effectively, problem-solve proactively, and maintain professionalism while managing multiple clinical trials and deadlines. Qualifications Minimum of 2–3 years of CLINICAL RESEARCH experience preferred Current GCP (Good Clinical Practice) training/certification required Medical office, nursing, allied health, or healthcare experience strongly preferred Prior experience coordinating pharmaceutical and/or device clinical trials Strong organizational, communication, and multitasking skills Ability to prioritize and manage multiple studies simultaneously Dependable, detail-oriented, and self-motivated Ability to work independently with minimal supervision Comfortable interacting with patients, sponsors, CROs, physicians, and monitors Proficiency with EMR systems, Microsoft Office, and electronic data entry systems Knowledge of IRB processes, informed consent, source documentation, adverse event reporting, and regulatory compliance Experience with recruitment, retention, and participant scheduling preferred Phlebotomy experience is a plus Bilingual candidates are encouraged to apply Responsibilities Coordinate and manage day-to-day clinical trial activities Screen, recruit, and retain study participants Conduct and document informed consent procedures Schedule and coordinate study visits and follow-up appointments Ensure protocol compliance and participant safety Maintain accurate source documentation, regulatory binders, and study records Enter and resolve data queries in electronic data capture systems Communicate effectively with sponsors, CROs, monitors, investigators, and participants Prepare for sponsor monitoring visits, audits, and site initiation visits Assist with lab processing, specimen handling, shipping, and study-related procedures Track enrollment goals, study timelines, visit windows, and regulatory deadlines Participate in occasional weekend community engagement and outreach events related to research and education Support a positive, professional, team-oriented environment focused on excellence and growth Application Requirements Current resume/CV List of clinical trials previously worked on Specific role/capacity on each study (Coordinator, Regulatory, Recruitment, Data Entry, etc.) Certifications and GCP training documentation Professional references Preferred Therapeutic Experience Neurology Migraine/Headache Medicine Alzheimer’s Disease/Dementia Psychiatry Internal Medicine or Primary Care We are seeking someone reliable, professional, organized, and committed to growing with a physician-led research program focused on innovation, patient care, and advancing clinical science. Competitive compensation will be based on experience and qualifications. #J-18808-Ljbffr Rehabilitation and Neurological Services, LLC