Assistant Clinical Research Coordinator- Neurology (Las Vegas, NV)

Profound Research
Las Vegas, NV
On-site

Who this role is best for

Geared toward entry-level candidates comfortable with on-site clinical trial coordination and patient engagement, in the neurology domain with potential for growth and hands-on learning.

Best fit for

  • Entry-level candidates eager to gain hands-on clinical trial experience and contribute directly to patient care.
    — “You’ll learn by doing – gaining hands-on experience in study coordination, patient interaction, data collection, and clinical procedures”
  • Individuals who thrive in collaborative settings and are driven by making a real-world impact in healthcare.
    — “contributing to research that has real-world impact from day one”

Things to consider

  • The role requires on-site presence and may involve travel between locations, which could affect work-life balance.
    — “Travel between company sites, meetings, or partner locations may be required”
  • Candidates should be prepared for a dynamic work environment with direct patient interaction.
    — “You’ll be present with patients, part of a team, and contributing to research that has real-world impact from day one”

How to stand out

  • Highlight experience with clinical procedures and patient engagement in your resume and interview responses.
    — “gaining hands-on experience in study coordination, patient interaction, data collection, and clinical procedures”
  • Emphasize your ability to manage multiple tasks and maintain attention to detail in trial coordination.
    — “supporting the coordination of active clinical trials, including patient visits, scheduling, and study-related procedures”
  • Demonstrate adaptability and willingness to work in a clinical setting with varied physical demands.
    — “This role is performed on-site at a clinical or office facility and requires prolonged periods of sitting, standing, or walking throughout the work environment”
Pace · SteadyCollaboration · HighAutonomy · MediumDecision Impact · Individual

Derived from job-description analysis by Serendipath's career intelligence engine.

What success looks like

  • Support the coordination of active clinical trials
  • Support patient visits, scheduling, and study-related procedures
  • Learn by doing in study coordination, patient interaction, data collection, and clinical procedures
Typical background
Detail-orientedExperience in clinical research

Skills & requirements

Required

Clinical Research CoordinationPatient Visits SchedulingStudy-related ProceduresData CollectionClinical Procedures

Stack & domain

Clinical Trials CoordinationPatient VisitsSchedulingStudy-related ProceduresData CollectionClinical ProceduresCommunicationTeamworkProblem-solvingClinical ResearchNeurology

About the role

Original posting from Profound Research via Lever

About Profound Research 

Profound Research partners with community physicians to offer clinical trials as a therapeutic option for their patients. We handle all infrastructure, regulatory compliance, and administrative operations so physicians can focus on patient care. Our model gives patients access to the newest therapies while maintaining the trusted patient-physician relationship.  

Our Mission: Improving Lives by Providing Advanced Therapeutic Options 

Our Vision: Creating the Absolute Best Patient-Physician Experience in Clinical Research 

Our Values:  

Compassion: We prioritize the patient-physician relationship, ensuring every interaction is service-oriented and patient-centered. 

Urgency: We work hard and practice selflessness, acting swiftly and decisively to meet the needs of our patients, partners, and colleagues.  

Solution Orientation: We embrace challenges with a positive mindset, communicate directly, and identify and implement effective solutions with efficiency.  

Excellence: We insist on excellence, holding ourselves accountable and empowering each other to deliver best-in-class service while maintaining the highest ethical and scientific standards.  

Start Your Career in Clinical Research 

If you’re curious about how new treatments reach patients, detail-oriented by nature, and energized by work that genuinely matters – this is where that career begins.  

As an Assistant Clinical Research Coordinator at Profound Research, you’ll work alongside experienced clinical research staff at one of our sites, supporting the day-to-day execution of clinical trials that give patients access to therapies they couldn’t otherwise reach. You’ll learn by doing – gaining hands-on experience in study coordination, patient interaction, data collection, and clinical procedures – with a clear path to grow into greater ownership and responsibility over time.  

This isn’t a behind-the-desk role. You’ll be present with patients, part of a team, and contributing to research that has real-world impact from day one.  

What You’ll Do 

Support the coordination of active clinical trials, including patient visits, scheduling, and study-related procedures 

Physical Requirements & Work Environment  

This role is performed on-site at a clinical or office facility and requires prolonged periods of sitting, standing, or walking throughout the work environment 

Requires the ability to communicate clearly in verbal and written forms and to read and interpret detailed materials

Must be able to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as needed

May be required to wear personal protective equipment (PPE) in accordance with facility protocols

Travel between company sites, meetings, or partner locations may be required

Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role  

Why Join Profound Research?

Source: Profound Research careers (Lever)

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