Director Of Nursing & Study Operations

Actalent; Richmond (VA); Presencial; USD 140 000 - 170 000; Tempo integral

Resumo da oferta

Actalent in Richmond, VA is seeking a Director of Nursing & Study Operations to lead nursing and clinical research operations, ensuring compliant, efficient, high-quality patient care and study conduct across departments.

This role oversees Clinical Research Coordinators, Medical Records/Data Coordinators, Clinic/Infusion Nurses, Nurse Navigators, and Referral teams. Requires RN, BSN, and 5+ years oncology leadership; onsite, full-time with competitive compensation.

Qualificações

• RN licensed in good standing.
• Bachelor's degree in Nursing or health-related field.
• Minimum 5 years of leadership experience in oncology clinical research.

Responsabilidades

• Provide proactive leadership to clinical and research coordinators and nursing staff.
• Deliver training, coaching and development for direct reports.
• Oversee patient-centered care and research delivery across workflows.
• Supervise referral intake, scheduling, patient navigation, and study startup processes.
• Ensure data capture accuracy and audit preparedness across departments.
• Maintain SOPs and drive continuous improvement of workflows.

Conhecimentos

RN license

BSN or higher

5+ years leadership

multidisciplinary leadership

clinical nursing experience

chemotherapy certification

ONS/ONCC/OCN

CITI GCP training

EHR/CTMS proficiency

MS Office proficiency

Formação académica

Bachelor's degree in Nursing or health-related field

Ferramentas

EHR systems

CTMS

Microsoft Office

Descrição da oferta de emprego

Job Title: Director of Nursing & Study Operations

Job Description

The Director of Nursing & Study Operations is a dual-function leadership role responsible for overseeing nursing teams and clinical research operations. This position ensures compliant, efficient, and high-quality patient care and study conduct across multiple departments, while supporting organizational goals for study growth, operational excellence, and patient-centered care. The Director leads Clinical Research Coordinators, Medical Records and Data Coordinators, Clinic and Infusion Nurses, Nurse Navigators, and Referral Intake and Scheduling teams, and works collaboratively with Quality, Regulatory, Finance, and Site Development functions.

Responsibilities

• Provide effective, proactive leadership to Clinical Research Coordinators, Data Coordinators, Medical Records staff, Clinic Nurses, Infusion Nurses, Nurse Navigators, Referral Intake and Scheduling teams.
• Deliver training, coaching, and ongoing professional development for direct reports to ensure competency and alignment with organizational values and expectations.
• Promote high-quality, patient-centered care and research delivery across clinical and study workflows.
• Oversee operational processes for referral intake, scheduling, patient navigation, study startup, and protocol feasibility assessments.
• Supervise implementation and utilization of clinical documentation systems, including CTMS and EHR platforms.
• Ensure accurate and timely data capture, monitor staff engagement, and maintain audit preparedness across all relevant departments.
• Oversee the use of effective workflows and standard operating procedures (SOPs), leading ongoing review and revision to improve efficiency and quality.
• Serve as a clinical and operational liaison to investigators, quality teams, regulatory departments, pharmacy, and global shared services.
• Partner with internal leaders to ensure compliant delivery of care within the scope of research protocols.
• Support the review and feasibility assessment of new protocols, with particular attention to nursing resources and operational capacity.
• Ensure equitable allocation of studies and provide ongoing support and guidance to study teams.
• Apply continuous improvement techniques to streamline workflows and resolve care or operational bottlenecks.
• Track and analyze key metrics related to referrals, screening, enrollment, and patient satisfaction to guide operational decisions.
• Participate in strategic initiatives and regional projects aimed at expanding access to clinical research and improving operational performance.
• Collaborate with quality and compliance teams to uphold all applicable federal clinical research regulations, Good Clinical Practice (GCP), and GDPR requirements.
• Perform other related duties as assigned to support nursing and study operations.

Essential Skills

• Registered Nurse (RN) license in good standing with the state.
• Bachelors degree in Nursing or a health-related field.
• Minimum 5 years of leadership experience in oncology clinical research.
• Strong management and leadership skills, with experience overseeing multidisciplinary clinical and research teams.
• Clinical nursing experience, including infusion and oncology care.
• Chemotherapy certification and oncology nursing expertise.
• ONS/ONCC certification and OCN certification.
• Demonstrated experience in clinical research operations, including study conduct and chart review.
• CITI GCP training and strong working knowledge of federal clinical research regulations, Good Clinical Practice (GCP), and GDPR.
• Proficiency with electronic health record (EHR) systems and clinical trial management systems (CTMS).
• Familiarity with Microsoft Office applications for documentation, communication, and data analysis.

Additional Skills & Qualifications

• Ability to provide coaching, mentorship, and professional development to diverse clinical and research teams.
• Strong analytical skills to track and interpret key operational metrics related to referrals, screening, enrollment, and patient satisfaction.
• Experience developing, implementing, and refining workflows and SOPs in clinical and research settings.
• Comfort working cross-functionally with Quality, Regulatory, Finance, Pharmacy, and Site Development teams.
• Strong communication and collaboration skills to serve as an effective liaison between clinical staff, investigators, and shared services.
• Commitment to patient-centered care and high-quality research delivery.
• Interest in contributing to the growth of clinical research and expanding access to innovative studies.

Work Environment

This is a full-time leadership role based in a clinical research setting, with standard hours of Monday through Friday, 8:00 a.m. to 5:00 p.m. The Director works in a multidisciplinary environment that includes clinic and infusion areas, medical records and data coordination functions, and research operations teams. The role involves regular collaboration with quality, regulatory, finance, pharmacy, and site development staff, and requires daily use of EHR systems, CTMS platforms, and Microsoft Office applications to manage workflows, documentation, and metrics. The environment is focused on delivering high-quality oncology care and clinical research, with opportunities to influence organizational growth and advance research initiatives.

Job Type & Location

This is a Permanent position based out of Richmond, VA.

Pay And Benefits

The pay range for this position is $140000.00 - $170000.00/yr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

will provide benefits to the candidate

Application Deadline

This position is anticipated to close on Oct 26, 2026.

Workplace Type

This is a fully onsite position in Richmond,VA.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [e-mail] for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.