Clinical Research Coordinator- Phase II-III - Full-Time - Wolf River - Registered Nurse (RN) Preferred

<p><strong>Job Title: </strong>Clinical Research Coordinator- Phase II-III</p> <p><strong>About Us</strong></p> <p>At West Cancer Center, we are dedicated to providing compassionate, patient-centered care while advancing groundbreaking research. Our team fosters collaboration, innovation, and professional growth, ensuring that every role contributes to making a difference in patients’ lives. Join us in our mission to provide comprehensive support to those navigating the challenges of cancer treatment.</p> <p><strong>Position Overview</strong></p> <p>The Clinical Research Coordinator plays a vital role in managing oncology patients participating in pharmaceutical-sponsored clinical trials. This position is responsible for patient screening, enrollment, education, and ongoing monitoring to ensure compliance with study protocols and regulatory standards. The ideal candidate will have prior experience managing clinical trials and a strong understanding of Good Clinical Practice (GCP) and FDA regulations.</p> <p><strong>Key Responsibilities</strong></p> <ul> <li>Recruit and screen potential clinical trial subjects</li> <li>Conduct detailed review of patient medical history and current findings for eligibility</li> <li>Educate nursing staff on proper administration and side effects of study therapies</li> <li>Educate patients on study protocols, medication adherence, and symptom management</li> <li>Act as a liaison between the Research Team and non-research clinical staff</li> <li>Maintain patient safety, rights, and informed consent throughout the study</li> <li>Ensure regulatory compliance and maintain current knowledge of the Code of Federal Regulations</li> <li>Monitor study progress and patient outcomes</li> <li>Interface with multiple departments, including Physicians, Nurses, Radiology, Medical Records, Laboratory, Insurance, and Pharmacy</li> <li>Document all relevant patient and study information accurately</li> <li>Maintain a professional demeanor and uphold confidentiality at all times</li> <li>Perform other duties as assigned</li> </ul> <p><strong>Qualifications</strong></p> <p><strong>Education &amp; Experience</strong></p> <ul> <li>Associate’s degree or equivalent from a two-year college or technical school</li> <li>Minimum of 1–2 years of related clinical research experience, or successful completion of 1 year as an Associate Clinical Research Coordinator I</li> <li><strong>Preferred:</strong> Registered Nurse (RN) certification</li> </ul> <p><strong>Skills &amp; Abilities</strong></p> <ul> <li>Strong organizational,