Dayton Center for Neurological Disorders (DCND), one of the largest physician owned and operated private practices in Ohio, is seeking a Clinical Research Coordinator to add to our Research Team. The Clinical Research Coordinator (CRC) is responsible for managing and coordinating the day-to-day operations of assigned clinical trials, ensuring that they are conducted ethically and in accordance with regulations and protocols. This is an outstanding opportunity to join a full-time (M-F, no holidays or weekends!) outpatient practice, collaborating with DCND, Inc. physicians, researchers, and other clinical staff. Our ideal candidate would be a licensed LPN or RN in the state of Ohio with prior research experience in a medical office.
About Us
At Dayton Center for Neurological Disorders (DCND), our work changes lives every day. Employees are united by a shared mission: delivering compassionate, evidence-based neurological care that improves function, independence, and quality of life for our patients and their families. Every role - clinical, administrative, or support - directly contributes to better outcomes and meaningful human impact. We strive to create a stable workplace with predictable expectations, fair practices, and a culture that respects employees' time, well-being, and personal commitments.
What We Offer
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Competitive Pay - The pay range for the Clinical Research Coordinator position is $25 to $35 per hour.
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Employer-Sponsored Health, Dental, and Vision Insurance
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Employer-Paid Life & Short Term Disability Insurance
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401(k) Retirement Plan with Company Matching up to 4% after your first year
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Profit-Sharing
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Generous Paid Time Off of 12 Days per year (prorated your first year) - increases based on years of service!
What We Require For This Role
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Bachelor's Degree - In a scientific, health-related or business field is preferred.
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Prior experience as a Research Coordinator in a Medical Office.
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Familiarity with Good Clinical Practice (GCP) and Institutional Review Board (IRB) requirements
Key Job Responsibilities
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Participant Recruitment & Management: Identifying, screening, and enrolling eligible participants, obtaining informed consent, and managing participant data.
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Data Collection & Management: Collecting, processing, and managing clinical data, ensuring accuracy and completeness, and preparing reports.
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Regulatory Compliance: Adhering to study protocols, institutional policies, and regulatory guidelines (e.g., GCP, IRB).
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Communication & Collaboration: Liaising with investigators, sponsors, and other healthcare professionals to ensure smooth trial operations.
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Monitoring & Reporting: Monitoring participant safety, reporting adverse events, and maintaining accurate research documentation.
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Study Logistics: Managing study supplies, equipment, and budgets, and coordinating with laboratories.
At Dayton Center for Neurological Disorders, we combine compassionate neurological care, collaborative teamwork, and professional growth to make a meaningful difference - for our patients and our people. Apply today to become a part of the DCND family!
