Posted 26 June, 2026

Job Id: 628968

Research Nurse


Location: Las Vegas, Nevada
Category: Nursing
Salary: Apply for details
Country: United States
Employment: Contract
Worksite: On-Site
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Job Description


 

Key Responsibilities

Patient Visit Delivery

  • Conduct off-site patient visits (home-based) in alignment with study protocol and timelines
  • Schedule and coordinate visits directly with the patient/carer
  • Perform visit activities including:
    • Vital signs collection
    • ECG acquisition
    • Blood sampling (PK/PD)
    • Cannulation and venipuncture
    • Adrenal insufficiency assessments
    • Investigational Product (IP) dispensing and accountability
    • Completion of electronic questionnaires
  • Ensure all visits are completed within required appointment windows

Clinical Documentation & Reporting

  • Accurately complete study worksheets and source documentation
  • Record all procedures, observations, and follow-up actions during visits
  • Submit documentation promptly for QC and site review
  • Maintain complete, audit-ready records at all times

Visit Preparation & Logistics

  • Prepare for each visit, ensuring all equipment and consumables are available, including:
    • ECG machine, centrifuge, BP monitor, weighing scale, measuring tape
    • PPE and blood/urine sampling supplies
  • Coordinate sample handling and shipment logistics
  • Organize required materials and ensure proper IP handling

Patient & Site Communication

  • Serve as primary point of contact for patient visit coordination
  • Liaise with investigator site staff for pre-visit handover (e.g., medications, adverse events)
  • Communicate visit findings and escalate adverse events immediately
  • Maintain professional and patient-centric communication at all times

Visit Follow-Up Activities

  • Complete post-visit documentation and resolve data queries
  • Ensure proper handling and return of biological samples and study materials
  • Maintain infection prevention and control standards
  • Confirm all activities and documentation are completed in line with protocol

Compliance & Quality

  • Adhere strictly to study protocol, SOPs, and ICH-GCP guidelines
  • Ensure compliance with regulatory, ethical, and safety requirements
  • Participate in audits, inspections, and quality activities as needed

Study & Team Engagement

  • Participate in required study-related activities including:
    • Study-specific training (1-3 hours)
    • Protocol familiarization and documentation review (~6 hours)
    • Site initiation visit (~2 hours)
    • Patient introduction visit (~1 hour)
  • Attend study meetings, calls, and provide status updates as required

Top Skills & Requirements

Clinical Expertise

  • Active Registered Nurse (RN) license
  • Strong clinical competencies including:
    • Venipuncture and cannulation
    • ECG acquisition
    • Vital signs and patient assessment
    • Sample processing (including centrifugation)
  • Experience with clinical trials, home visits, or decentralized trials preferred

Regulatory & Compliance

  • Current GCP certification (within 2 years)
  • Valid Basic Life Support (BLS) certification
  • Strong understanding of clinical trial protocols and safety reporting (AE/SAE)

Operational Skills

  • Ability to independently manage visit schedules and logistics
  • Strong attention to detail in documentation and data accuracy
  • Experience with electronic data capture tools and systems
  • Ability to manage travel, visit timing, and administrative requirements effectively

Communication & Interpersonal Skills

  • Strong patient-facing communication and bedside manner
  • Ability to coordinate effectively with remote study teams and sites
  • Clear, timely communication of clinical findings and issues

Additional Requirements

  • Ability to travel to patient homes (local travel required)
  • Valid driver’s license and reliable transportation
  • Comfortable working independently in a home-based care setting
  • Flexible to accommodate visit timing and study needs

Equal Opportunity Employer

We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.

Fraud Alert

Candidate safety is a top priority at Planet Pharma. The industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly, never provide banking information during the application process and always double check the email address of the Recruiter to ensure it’s from an official Planet Pharma domain (@planet-pharma.com, @planet-pharma.co.uk, and @ppgadvisorypartners.com) and not a domain with an alternative extension like .net, .org or .jobs.

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