A Director of Nursing manages and supervises all nursing staff at a hospital or long term care facility. Manages communications with physicians, manages budgets and expenses, and assists other administrators with managing operations. Monitors staff schedules and the quality of nursing care at the facility. Maintains professional license or certification requirements.
Director, Nursing & Study Operations START Center for Cancer Research - 3.0 Richmond, VA Job Details 14 hours ago Benefits Disability insurance Health insurance Dental insurance Flexible spending account Paid time off Vision insurance 401(k) matching Flexible schedule Qualifications Nursing RN License GDPR compliance expertise Bachelor's degree Managing clinical research teams Oncology research
ONS/ONCC
Chemotherapy Immunotherapy Certificate Productivity software Collaborative Institutional Training Initiative Certification (CITI) Clinical quality assurance standards Oncology Healthcare compliance Nursing Full Job Description The START Center for Cancer Research ("START") is the world's largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering "Hope Through Access" to cutting edge trials throughout the United States and Europe. The START Center for Cancer Research is seeking a Director of Nursing & Study Operations. The Director of Nursing & Study Operations is a dual-function leadership role responsible for the oversight and performance of START's nursing teams and clinical research operations. This role ensures compliant, efficient, and high-quality care and study conduct across departments, while supporting START's goals for study growth, operational excellence, and patient care. The Director leads Clinical Research Coordinators, Medical Records, Data Coordinators, Clinic Nurses, Infusion Nurses, Nurse Navigators, Referral Intake and Scheduling teams. The position works collaboratively across departments including Quality, Regulatory, Finance, and Site Development.
Location:
START Richmond Work Schedule:
Monday-Friday 8:00am-5:00pm Essential Responsibilities Leadership & Oversight Provide effective, proactive leadership to Clinical Research Coordinators, Data Coordinators, Medical Records staff, Clinic Nurses, Infusion Nurses, Nurse Navigators, Referral Intake and Schedulers. Provide training, coaching, and development for direct reports, ensuring ongoing competency and alignment with START's values and expectations. Promote high-quality, patient-centered care and research delivery across clinical and study workflows. Operational Management Oversee processes for referral intake, scheduling, patient navigation, study startup, and protocol feasibility. Supervise implementation of CTMS, EHR, and other clinical documentation systems. Ensure accurate and timely data capture, monitor engagement, and audit preparedness across departments. Oversee use of effective workflows and SOPs; lead ongoing review and revision efforts. Clinical & Study Collaboration Serve as clinical and operational liaison to investigators, quality team, regulatory, pharmacy, and global shared services. Partner with leaders to ensure compliant delivery of care within the scope of research protocols. Support review and feasibility assessment of new protocols with attention to nursing and operational capacity. Ensure equitable study allocation and ongoing support for study teams. Process Improvement & Strategic Support Use continuous improvement techniques to streamline workflows and resolve care or operational bottlenecks. Track key metrics across referrals, screening, enrollment, and patient satisfaction. Participate in strategic initiatives and regional projects to expand access and improve operational performance. Collaborate with quality and compliance teams to uphold all applicable federal, GCP, and GDPR regulations. Other duties may be assigned at any time.
Required Education and Experience:
Bachelor's degree in Nursing or Health-related field RN license in good standing with state Minimum 5 years of leadership experience in oncology clinical research
CITI GCP
training Strong working knowledge of federal clinical research regulations, GCP, and GDPR Familiarity with Microsoft Office applications and
Approximately 80% of time is spent sitting Very fast-paced and ever-changing healthcare environment Demanding deadlines and constant knowledge updates required Works closely with physicians and cross-functional teams Intermittent travel to support site activation and training (
