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

Profound Research•Las Vegas, NV

12d•Onsite

About The Position

Profound Research is hiring an Assistant Clinical Research Coordinator to support clinical trials at its Las Vegas, Nevada site. The role offers hands-on experience in study coordination, patient interaction, data collection, and clinical procedures while working alongside experienced clinical research staff. The position is patient-facing and contributes to research that expands access to therapies and advances medical knowledge. The successful candidate will develop clinical research skills and may grow into greater ownership and responsibility over time. The role is performed on-site at a clinical or office facility. It involves prolonged periods of sitting, standing, or walking; communicating verbally and in writing; reading and interpreting detailed materials; navigating a clinical facility, including limited-space areas; and transporting supplies or work materials as needed. Personal protective equipment may be required under facility protocols, and travel between company sites, meetings, or partner locations may be required. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.

Requirements

High school diploma or technical degree and 3 or more years of relevant experience in life sciences; or an associate degree and 1 or more year of relevant experience; or a bachelor's degree with relevant coursework or experience in a clinical or life sciences setting.
Clear communication, attention to detail, ownership of work, and genuine care for the patient experience.
Comfort working in a fast-paced, team-based environment.
Proficiency with standard computer tools and ability to learn new systems quickly.
ICH-GCP and IATA certification required within a defined timeframe after hire.

Nice To Haves

Familiarity with medical terminology and basic clinical procedures.

Responsibilities

Support the coordination of active clinical trials, including patient visits, scheduling, and study-related procedures.
Assist with data collection and documentation while following clinical research standards.
Perform and develop competency in clinical procedures, including vital signs, EKGs, phlebotomy, and specimen processing.
Interact directly with study participants, greet them, explain visit steps, and support them throughout the process.
Work with Clinical Research Coordinators and site leadership, seeking feedback and building clinical knowledge.
Follow established protocols, SOPs, and Good Documentation Practices to help maintain a compliant, audit-ready site.