Clinical Research Coordinator - Full-Time - Wolf River

Job Title: Clinical Research CoordinatorAbout UsAt 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.Position OverviewThe 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.Key ResponsibilitiesRecruit and screen potential clinical trial subjectsConduct detailed review of patient medical history and current findings for eligibilityEducate nursing staff on proper administration and side effects of study therapiesEducate patients on study protocols, medication adherence, and symptom managementAct as a liaison between the Research Team and non-research clinical staffMaintain patient safety, rights, and informed consent throughout the studyEnsure regulatory compliance and maintain current knowledge of the Code of Federal RegulationsMonitor study progress and patient outcomesInterface with multiple departments, including Physicians, Nurses, Radiology, Medical Records, Laboratory, Insurance, and PharmacyDocument all relevant patient and study information accuratelyMaintain a professional demeanor and uphold confidentiality at all timesPerform other duties as assignedQualificationsEducation & ExperienceAssociate’s degree or equivalent from a two-year college or technical schoolMinimum of 1–2 years of related clinical research experience, or successful completion of 1 year as an Associate Clinical Research Coordinator IPreferred: Registered Nurse (RN) certificationSkills & AbilitiesStrong organizational, follow-up, and problem-solving skillsExcellent verbal and written communication abilitiesAbility to manage multiple priorities in a fast-paced environmentProficiency in computer applications, including word processing and emailAbility to collaborate effectively within multidisciplinary teamsStrong knowledge of clinical research regulations, data management, and patient safetyComfort working near potentially hazardous materialsAbility to analyze complex data and interpret technical documentsCompetence in performing necessary calculations (BSA, ANC, drug dosing)Ability to travel as requiredWhy West Cancer Center is a Great Place to WorkMeaningful Impact: Play a direct role in supporting patients through one of the most challenging times of their lives.Collaborative Culture: Work alongside a multidisciplinary team of dedicated professionals committed to improving cancer care.Professional Development: Benefit from ongoing training, educational resources, and growth opportunities.Mission-Driven Environment: Be part of an organization guided by compassion, integrity, and innovation.No Nights, Weekends, Or Holidays. Comprehensive Benefits Package.Join UsIf you are a detail-oriented clinical research professional looking to make a difference in oncology care, apply today to become a Clinical Research Coordinator at West Cancer Center.