Nursing Internship- Summer 2026

DEKA Research & Development • Manchester, NH

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About The Position

DEKA Research & Development is seeking a Nursing Intern who will support the SAFEflow commercialization team by contributing clinical knowledge to real-world evaluation activities. Additionally, this intern will be collaborating and supporting the SAFEflow Clinical Team in executing user training, designing an approach to data collection and analysis, and support the provision of post-implementation monitoring. This role will bridge clinical practice and industry, while gaining hands-on exposure on how medical devices are introduced, evaluated, and optimized in real healthcare settings. The intern will also provide ad hoc clinical inputs to the DEKA R&D Engineering Team on an as needed basis. DEKA offers Internships and Co-Ops for full time students (must be at least 18 years of age). Internships last a minimum of 10 weeks, 12 preferred. All summer internships must start no later than June 15, 2026. How you will make an impact as a Nursing Intern: Support real-world evaluation (RWE) of the SAFEflow Infusion System by: Assisting with clinical workflow assessments, assisting in the design of data collection tools, and providing support for data analysis suitable for publication. Supporting the execution and delivery of training materials for clinicians and healthcare staff (e.g., in-services, user guides, and quick reference tools). Participating in device implementation activities at clinical sites, including onboarding, workflow integration, and go-live support. Observing and documenting device usage using prescribed tools and processes to facilitate staff feedback, assess usability, safety, and workflow optimization opportunities. Supporting monitoring of device performance, user feedback, and clinical outcomes in collaboration with clinical and commercial teams. Assist with preparation of reports, presentations, and summaries for internal /external stakeholders. Collaborate with cross-functional teams including engineering, product management, sales, and regulatory/quality. Ensure activities align with patient safety, clinical best practices, and regulatory requirements Demonstrate professionalism and confidentiality when interacting with internal and external stakeholders and clinical partners, patient-related data, and project related information.

Requirements

• Current enrollment in an accredited nursing program (BSN or MSN) or related health sciences program local to Manchester, NH.
• Completion of foundational clinical coursework.
• Strong interest in medical devices, innovation, or healthcare technology.
• Excellent communication, organization, and documentation skills.

Nice To Haves

• Clinical experience in acute care, ambulatory care, or specialty settings relevant to infusion devices.
• Familiarity with evidence-based practice or quality improvement initiatives.
• Comfort using Microsoft Office and similar tools.

Responsibilities

• Support real-world evaluation (RWE) of the SAFEflow Infusion System by: Assisting with clinical workflow assessments, assisting in the design of data collection tools, and providing support for data analysis suitable for publication.
• Supporting the execution and delivery of training materials for clinicians and healthcare staff (e.g., in-services, user guides, and quick reference tools).
• Participating in device implementation activities at clinical sites, including onboarding, workflow integration, and go-live support.
• Observing and documenting device usage using prescribed tools and processes to facilitate staff feedback, assess usability, safety, and workflow optimization opportunities.
• Supporting monitoring of device performance, user feedback, and clinical outcomes in collaboration with clinical and commercial teams.
• Assist with preparation of reports, presentations, and summaries for internal /external stakeholders.
• Collaborate with cross-functional teams including engineering, product management, sales, and regulatory/quality.
• Ensure activities align with patient safety, clinical best practices, and regulatory requirements
• Demonstrate professionalism and confidentiality when interacting with internal and external stakeholders and clinical partners, patient-related data, and project related information.

What This Job Offers

• Job Type: Full-time
• Career Level: Intern