Director of Research Nursing - Full Time - Wolf River

Job Title: Director of Research NursingAbout UsAt West Cancer Center, we are committed to advancing innovative cancer research while delivering compassionate, patient-centered care. Our research teams play a critical role in expanding treatment opportunities and improving outcomes for patients through cutting-edge clinical trials and collaborative research initiatives.Position OverviewThe Director, Research Nursing oversees research nursing and clinical operations staff while ensuring high-quality execution of clinical research studies, regulatory compliance, patient safety, operational efficiency, and sponsor satisfaction. This role collaborates closely with investigators, sponsors, CROs, regulatory personnel, and executive leadership to support study activation, enrollment, quality assurance initiatives, and continued program growth. The Director is responsible for developing operational processes, mentoring research personnel, and ensuring adherence to FDA regulations, ICH-GCP guidelines, sponsor requirements, and organizational policies. This role serves as a key leader in advancing research excellence, quality outcomes, and strategic program development.Key ResponsibilitiesOversees and supervises research personnelRecruits, hires, supervises, evaluates, disciplines, and assists in terminations of research staffOversees work schedules for clinical research personnel and monitors productivityEnsures compliance of research operations with federal and state regulationsWorks closely with Principal Investigators for study start-up, Site Initiation Visits (SIVs), and subject identification strategiesImplements, revises, communicates, and monitors Standard Operating Procedures (SOPs) for the Research DepartmentPresides at staff meetings and research meetings as requiredServes as liaison to internal departments for issue resolutionPlans and implements training and educational opportunities for research personnelGuides and motivates physicians, administration, peers, and subordinates in supporting research operationsInterfaces with all departments regarding integration of research processesInterfaces with pharmaceutical companies, sponsors, and contract research organizations (CROs)Provides operational quality oversight for research personnel by performing routine chart audits, monitoring protocol adherence, and identifying opportunities for process improvement and compliance enhancementReviews quality metrics, protocol deviations, CAPAs, audit findings, and monitoring trends to identify opportunities for process improvementPartners with Regulatory Affairs and operational leadership to ensure inspection readiness and continuous quality improvement initiativesEnsures research personnel maintain required training, competencies, and compliance documentationOversees implementation and adherence to departmental Standard Operating Procedures (SOPs)Leads process improvement initiatives to optimize operational efficiency, protocol compliance, and research quality standardsMaintains professionalism, confidentiality, and ethical standards in all interactionsComplies with organizational safety policies and proceduresPerforms all other duties as assignedQualificationsEducation & ExperienceRequired:Master’s degree with two years of related experience; OR Bachelor’s degree with four years of related experience; OR seven to ten years of related experience and/or training; OR equivalent combination of education and experienceStrong knowledge of FDA regulations, ICH-GCP guidelines, and clinical research operationsExcellent organizational and follow-up skillsStrong verbal and written communication skillsStrong problem-solving and critical-thinking abilitiesAbility to organize and prioritize work assignments in a fast-paced environmentAbility to participate in multidisciplinary teams and maintain effective professional relationshipsProficient in Microsoft Office applications including Word, Outlook, Excel, and email systemsAdditional hours may be requiredCredential/LicensureRequired:Current RN license requiredWork Environment & Physical DemandsTypical clinical and office environment with moderate noise levelAbility to walk, sit, use hands/wrists, talk, hear, and see for extended periods of timeAbility to work near toxic or caustic chemicalsAbility to read, analyze, and interpret financial reports, government regulations, scientific journals, and legal documentsAbility to communicate effectively verbally and in writing with leadership, employees, regulatory agencies, and external stakeholdersAbility to calculate figures and perform basic algebra and geometry applicationsAbility to define problems, collect data, establish facts, and draw valid conclusionsAbility to interpret complex technical instructions and manage multiple variablesAbility to lift up to 10 poundsOccasional travel may be 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 passionate clinical research leader with strong operational expertise and a commitment to advancing oncology research, we encourage you to apply for the Director, Research Nursing position at West Cancer Center.