Clinical Research Coordinator in Centerville, Ohio at Dayton Center For Neurological Disorders Inc

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

• Competitive Pay - The pay range for the Clinical Research Coordinator position is $25 to $35 per hour.
• Employer-Sponsored Health, Dental, and Vision Insurance
• Employer-Paid Life & Short Term Disability Insurance
• 401(k) Retirement Plan with Company Matching up to 4% after your first year
• Profit-Sharing
• 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

• Bachelor's Degree - In a scientific, health-related or business field is preferred.
• Prior experience as a Research Coordinator in a Medical Office.
• Familiarity with Good Clinical Practice (GCP) and Institutional Review Board (IRB) requirements

Key Job Responsibilities

• Participant Recruitment & Management: Identifying, screening, and enrolling eligible participants, obtaining informed consent, and managing participant data.
• Data Collection & Management: Collecting, processing, and managing clinical data, ensuring accuracy and completeness, and preparing reports.
• Regulatory Compliance: Adhering to study protocols, institutional policies, and regulatory guidelines (e.g., GCP, IRB).
• Communication & Collaboration: Liaising with investigators, sponsors, and other healthcare professionals to ensure smooth trial operations.
• Monitoring & Reporting: Monitoring participant safety, reporting adverse events, and maintaining accurate research documentation.
• 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!