Clinical Research Coordinator (CRC)

Job Description Position Summary We are seeking a highly motivated and detail-oriented Clinical Research Coordinator (CRC) to oversee and manage clinical trials from start-up through close-out. This role requires strong organizational skills, regulatory knowledge, and the ability to work closely with patients, investigators, sponsors, and coordinate activities across both on-site and remote PRN staff. Candidates must be willing to travel, including attendance at Investigator Meetings (IMs), as required. This is not an entry-level role and requires a high level of accountability, ownership, and the ability to operate independently with minimal oversight. Key Responsibilities Independently coordinate multiple clinical trials fromstartup to close-out Lead patient recruitment, screening, consenting, and retention strategies Conduct study visits, assessments, and protocol-specific procedures Ensurestrict adherence to GCP, FDA regulations, and protocol requirements Maintain high-qualitysource documentation and EDC data entry(real-time, audit-ready) Manage investigational product accountability and study logistics Serve as theprimary point of contactfor sponsors, CROs, and monitors Prepare for and confidently supportmonitoring visits, audits, and FDA inspections Identify inefficiencies and proactively improve workflows Performance Expectations Maintain audit-ready documentation at all times (ALCOA+ compliant) Ensure timely and accurate EDC data entry (real-time or within defined timelines) Demonstrate ownership of assigned studies with minimal oversight Maintain readiness for monitoring visits, audits, and FDA inspections at all times Proactively identify, document, and elevate issues, risks, and protocol deviations Work Environment Fast-paced, high-accountability clinical research setting Requires ability to manage competing priorities and adapt to changing study demands High level of autonomy with expectation of independent problem-solving Qualifications Bachelor’s degree in life sciences, healthcare, or related field (preferred) 2+ years of clinical research experience (CRC experience preferred) Strong knowledge ofGCP, FDA, and IRB processes Experience with EDC systems and clinical trial documentation Excellent organizational, communication, and multitasking skills Ability to manage multiple studies in a fast-paced environment Highly Preferred (but not required) Experience inneurology, neuromuscular, or rare disease trials Experience inindustry-sponsored trials Phlebotomy and/or clinical skills Certification (CCRC, CCRP, or equivalent) Experience in reviewing patient medical records for pre-screening Experience with CRIO preferred but not required Compensation & Benefits Competitive salary (based on experience; typical CRC range (~$50K-$70K/year) Health, dental, and vision insurance Paid time off Opportunities for growth and leadership within a rapidly expanding research center Company Description Neurology Rare Disease Center is a growing neurology and clinical research centre dedicated to advancing care for patients with rare neuromuscular diseases. We are committed to high-quality, patient-centred research and innovation. We are building a team of people who care deeply about patients and take pride in doing things the right way. #J-18808-Ljbffr Neurology Rare Disease Center