Clinical Research Associate Jobs in Nevada, United States

The FSP team seeks a Clinical Research Associate 2 to support clinical trials on the West Coast or in Texas. This role involves comprehensive site monitoring, data integrity verification, and adverse event reporting to ensure participant safety and protocol compliance.

Clinical Operations at Worldwide Clinical Trials drives innovative therapeutic research across neuroscience and psychedelics. The Senior Clinical Research Associate manages site activities, conducts study initiation visits, ensures regulatory compliance, and supports contract and budget negotiations.

Clinical Operations at Worldwide Clinical Trials drives scientific breakthroughs across therapeutic areas, including neuroscience and rare diseases. The Senior Clinical Research Associate manages site activities, conducts study initiation visits, and ensures regulatory compliance while supporting contracts, training, and safety reporting.

Fortrea is seeking Experienced CRA 2s to lead and support its Full Service Outsourcing team across major US hub locations. In this role, you will apply clinical judgement to monitor clinical trial sites, ensure participant safety and data integrity, and respond to emergencies per clinical research standards.

Fortrea’s Monitoring Excellence Academy is hiring Clinical Research Associates (CRA 1) for Oncology, CAR T, or Ophthalmology trials. The role involves site monitoring, data integrity verification, SAE reporting, and supporting study site operations across Central or West coast US hubs or Montreal, Canada.

FSP team at Covance seeks Senior Clinical Research Associate 2 to lead monitoring of in‑vitro diagnostics trials across the US. The role conducts site monitoring, data verification, SAE reporting and supports site staff training while ensuring protocol compliance. Remote work from any US location with 50‑60% overnight travel required.

Thermo Fisher Scientific seeks a Clinical Research Manager in Las Vegas to oversee clinical trials for patient and healthy subject populations. This on-site role involves managing study operations, serving as a liaison between internal teams and investigators, and ensuring regulatory compliance with FDA and ICH GCP guidelines.

Office of Clinical Trials, Research Department, Kirk Kerkorian School of Medicine (ADTO) ensures regulatory compliance for clinical research studies. The Coordinator prepares, submits, and maintains regulatory documents, acting as the primary liaison with IRBs, sponsors, and agencies while supporting investigators.

Starling Oncology (NASDAQ: STLN) is a community-based oncology network delivering specialized, value-based cancer care across five states. The Medical Director of Oncology Clinical Research will provide physician leadership for the clinical research program, expand patient access to clinical trials, and strengthen Principal Investigator oversight while maintaining an active Hematology & Oncology practice.

ThermoFisher Scientific's PPD clinical research portfolio seeks a Traveling Research Associate II to support clinic operations, manage patient care workflows, and ensure regulatory compliance across clinical trial sites. Day-to-day duties include performing technical and non-technical clinic procedures (vital signs, phlebotomy, urine collection, sleep testing), preparing and calibrating equipment, managing clinical supplies and specimen documentation, screening subjects per protocol, liaising wi

The Desert Research Institute’s Division of Hydrologic Sciences is seeking an Associate Research Professor to establish and lead an externally-funded research team advancing hydrologic science in arid environments, initially focused on Southern Nevada water resources research and supported in part by the Sulo and Aileen Maki Endowment. Day-to-day, the role develops and applies hydrologic and hydraulic models of surface and subsurface water movement, builds a Las Vegas-based research team, collab

Elsevier Clinical Content Team creates evidence‑based nursing reference material. The Associate Clinical Editor reviews, updates, and revises assigned content, ensures accuracy to clinical guidelines, and collaborates with internal teams to address content needs.

Elsevier Clinical Content Team builds and maintains evidence‑based nursing reference material. The Associate Clinical Editor reviews, updates and revises assigned content, ensures accuracy to current practice guidelines, and manages project timelines while collaborating with internal teams and responding to clinical inquiries.

UNLV School of Dental Medicine seeks a full‑time, 12‑month Faculty‑In‑Residence of Clinical Sciences (Endodontics) to lead the pre‑doctoral endodontic curriculum, supervise clinical and pre‑clinical courses, and provide patient care in both general dentistry and specialty clinics. The role supports Advanced Education programs in General Practice Residency, Pediatric Dentistry, and Orthodontics, and offers opportunities for intramural faculty practice and extramural private practice.

The University of Nevada, Las Vegas invites applications for General Dentist, Assistant/Associate/Professor in Residence, Department of Clinical Sciences, School of Dental Medicine. Successful candidates will provide comprehensive clinical supervision, oversight, and instruction in the delivery of safe, ethical, and evidence-based patient care by students enrolled in the DMD/DDS predoctoral dental program.

Elko Veterinary Clinic, part of AmeriVet, seeks an Associate Veterinarian to provide general, urgent, and emergency care for a diverse caseload in Northeastern Nevada. The role involves performing advanced orthopedic procedures with mentorship opportunities while collaborating with a supportive team.

UNLV Research Cyberinfrastructure team empowers researchers with advanced computing resources and services. The engineer installs, configures, and maintains HPC hardware, software, storage, and networking, while providing support and training to faculty and students.

Human Research Protection Program (HRPP) Education and Accreditation Manager at UNLV leads compliance and education for human subjects research. Works with HRPP leadership to design, implement, and evaluate training, SOPs, and accreditation processes.