Director of Nursing

The START Center for Cancer Research; Atlanta (GA); Presencial; USD 140.000 - 170.000; Tempo integral

Benefícios oferecidos por esta vaga

401(k) retirement plan with employer

Annual performance bonus

Generous paid time off and holidays

Medical, dental, and vision coverage

Company-paid life and disability保险

Employee Assistance Program (EAP)

Flexible spending accounts (FSA) and H

Resumo da vaga

The START Center for Cancer Research in Atlanta, GA seeks a Director of Nursing to oversee clinic nurses, infusion nurses, nurse navigators, and schedulers, ensuring high-quality care within oncology clinical trials.

You will lead training, ensure SOP compliance, coordinate patient care with study teams, and support coordinators. This role requires Mon-Fri 8:00 AM–5:00 PM with up to 5% travel and a commitment to continuous improvement.

Qualificações

• Bachelor’s degree in nursing is required.
• RN license in good standing with state required.
• ONS/ONCC chemotherapy immunotherapy certificate course required.
• Knowledge of GCP, GDPR and federal clinical research regulations required in US and Europe.
• Proficiency with Microsoft Office applications and clinical documentation systems.

Responsabilidades

• Provide effective leadership to managers, clinic nurses, infusion nurses, nurse navigators, schedulers, and referral intake coordinators.
• Provide training and ensure competency of staff and management.
• Maintain adherence to SOPs and participate in ongoing review and updates.
• Ensure high quality, coordinated care by communicating care plans to patients and scheduling timely visits.
• Provide clinical support and guidance for study coordinators and treatment room nurses.
• Serve as nurse educator/preceptor for new clinical research staff.
• Develop and deploy training to support compliance with internal standards.
• Ensure departments use efficient processes to support patient care within research protocols.
• Use process improvement techniques to identify and address care delivery gaps.
• Review incoming protocols for feasibility with respect to nursing operations and allocate studies accordingly.
• Track metrics for referral intake, new patient visits, enrollment, and screening in research processes.
• Lead enrollment growth efforts and remove barriers to patient visits and accruals.
• Coordinate with regulatory, quality, site development, pharmacy and finance to ensure compliance with federal and GCP requirements.
• Support implementation of CTMS, EHR and other systems for accurate documentation and data capture.

Conhecimentos

Leadership and team supervision

Process improvement

Regulatory/compliance knowledge

Communication with cross-functional团队

GCP knowledge

Formação

Bachelor’s degree in nursing

RN license in good standing

ONS/ONCC chemotherapy immunotherapy certificate course

Ferramentas

Microsoft Office

Clinical documentation systems

Descrição da vaga

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.

We are seeking a Director of Nursing to provide supervision to all clinic nurses, infusion nurses, nurse navigators, referral intake team and schedulers. The Director of Nursing provides professional guidance and development to the nurses and staff that he/she supervises, ensures organizational goals and objectives are met by the departments under their responsibility, and ensures on-going training, education and high-quality care are delivered through effective processes and systems in his/her respective departments.

Work Schedule: Monday through Friday, 8:00 AM to 5:00 PM. Schedule flexibility is required based on patient needs, business operations.

Location: Atlanta, Georgia

Essential Responsibilities

• Provide effective, proactive leadership to team members, including but not limited to managers, clinic nurses, infusion nurses, nurse navigators, schedulers, and referral intake coordinators.
• Provide effective training and ensure competency of staff and management team for respective job roles.
• Maintain adherence and demonstrate ongoing compliance for all departments with internal standard operating procedures and participate in ongoing review and updates as needed for the good of the patients, sponsors and organization.
• Ensure high quality, coordinated care by communicating care plans and schedules to patients, return patient calls promptly and provide same-day/ next day visits for patients with time-sensitive issues.
• Provide clinical support and guidance for study coordinators, primary nurses, and treatment room nurses.
• Serve as nurse educator / preceptor for new clinical research staff, including treatment room nurses, triage LVNs, primary nurses and study coordinators.
• Develop and deploy necessary training and education to support compliance with internal quality standards.
• Ensure departments are using efficient, effective processes and systems to support patient care workflows and compliant care delivery in the context of clinical research protocols.
• Use continuous process improvement techniques to proactively identify and address areas of improvement for the good of the patient and the organization.
• Review all incoming protocols for feasibility with respect to nursing operations and study coordinator teams. Manage study allocation equitably across study coordinator team members.
• Track and maintain effective standards and metrics with respect to referral intake, new patient visit, enrollment, and screening steps in research process.
• Lead efforts related to growth in enrollment; identify and prevent any barriers to new patient visits and enrollment.
• Ensure effective inter-departmental interaction and communication with other support departments including regulatory, quality, site development, pharmacy and finance to ensure successful care delivery and compliance with all federal, GCP and regulatory agency requirements.
• Support effective use and implementation of CTMS system, EHR system, and other necessary software to ensure appropriate and accurate documentation and data capture in the departments of responsibility.
• Supervise nurse navigators and support growth goals of clinical research program with respect to new patient referrals and accruals.

Required Education And Experience

• Bachelor’s degree in nursing.
• RN license in good standing with state.
• ONS/ONCC chemotherapy immunotherapy certificate course.
• Knowledge of GCP, GDPR and federal clinical research regulations required in US and Europe.
• Must be familiar with Microsoft Office applications and clinical documentation systems.

Preferred Education And Experience

• Advanced degree in nursing or leadership.
• Oncology Certified Nurse (OCN).
• Previous experience in oncology clinical research.

Physical And Travel Requirements

• Required to travel up to 5% of the time.
• Approximately 80% of time is spent sitting.
• Very fast-paced and ever-changing healthcare environment.
• Demanding deadlines and time frames.
• Constant demand for updating knowledge.
• Works closely with physicians and ancillary personnel in caring for and treating oncology/hematology patients.

Best-in-Class Benefits and Perks

Benefits

We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package—based on experience—along with comprehensive benefits designed to support you both personally and professionally:

• 401(k) retirement savings plan with employer match
• Eligibility for an annual performance bonus, based on role and company results
• Generous paid time off and paid holidays
• Comprehensive medical, dental, and vision coverage and optional insurance options
• Company paid life and disability insurance for added financial protection
• Employee Assistance Program (EAP) providing confidential, no ‑cost support for you and your family from day one
• Flexible FSA and HSA plans to support your financial wellness
• Commitment to a supportive environment that values balance, wellbeing, and flexibility
• We’re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you’ll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation.

More About START

START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world’s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of “Hope Through Access”.

Learn more atSTARTresearch.com.

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.