Nurse Practitioner Jobs

About The Position

Requirements

• Master's or Doctoral degree in Nursing from an accredited Nurse Practitioner program
• Current, unrestricted NP license in South Dakota; national certification (e.g., ANCC, AANP)
• Active DEA registration (or eligibility to obtain)
• 1–3 years of clinical experience as an NP
• Strong assessment, documentation, and communication skills
• Ability to work collaboratively within a multidisciplinary research team

Nice To Haves

• Prior experience in clinical trials, either in a clinical or coordinator-facing capacity, or a research-intensive clinical setting
• Familiarity with delegation-of-authority logs, GCP, IRB processes, and FDA regulatory requirements
• CCRP, CCRC, or similar clinical research certification (or willingness to obtain)
• Comfort working across both clinical and administrative/operational tasks as the site's needs require
• Experience with electronic data capture (EDC) systems and electronic health records (EHR)

Responsibilities

• Perform study visits, including history and physical exams, symptom assessments, and protocol-required evaluations, per delegation of authority
• Support clinical eligibility determinations for screening and enrollment
• Identify, assess, document, and report adverse events (AEs) and serious adverse events (SAEs) within regulatory timelines
• Order, review, and act on laboratory results, diagnostics, and other protocol-specified assessments
• Administer or oversee administration of investigational product per protocol
• Sign off on source documents and regulatory paperwork where delegated
• Represent the site during sponsor visits, monitoring visits, audits, or inspections as designated
• Assist with participant scheduling, visit logistics, and protocol calendars, particularly to help cover gaps in coordinator availability
• Support data entry into EDC systems and resolution of sponsor/monitor queries
• Assist with informed consent process, participant education, and retention efforts
• Help maintain drug/device accountability logs and regulatory binders
• Maintain accurate and complete source documentation and case report forms (CRFs)
• Ensure all activities comply with FDA regulations, ICH-GCP guidelines, IRB requirements, and institutional SOPs
• Collaborate closely with the PI, other clinical staff, CRCs, and sponsor/CRO representatives
• Support protocol feasibility review and study start-up activities as needed