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Clinical Study Assistant Jobs in Nevada (NOW HIRING)

Monitor the collection of urine and, when required, fecal specimens from subjects participating in clinical studies to ensure compliance with study procedures. * Assist with urine collection from ...

Monitor the collection of urine and, when required, fecal specimens from subjects participating in clinical studies to ensure compliance with study procedures. * Assist with urine collection from ...

Clinical Research Coordinator

Las Vegas, NV ยท On-site

$23.25 - $30.75/hr

Clinical Research Coordinator Location: Las Vegas, NV Onsite Hours/Schedule : 40 hours Type ... study participants. * Assist with informed consent and enrollment of study participants in ...

Clinical Research Coordinator

Las Vegas, NV ยท On-site

$23.25 - $30.75/hr

Clinical Research Coordinator Location: Las Vegas, NV Onsite Hours/Schedule : 40 hours Type ... study participants. * Assist with informed consent and enrollment of study participants in ...

Clinical Research Coordinator

Las Vegas, NV ยท On-site

$23.25 - $30.75/hr

Clinical Research Coordinator Location: Las Vegas, NV Onsite Hours/Schedule : 40 hours Type ... study participants. * Assist with informed consent and enrollment of study participants in ...

Clinical Research Coordinator

Las Vegas, NV ยท On-site

$23.25 - $30.75/hr

Clinical Research Coordinator Location: Las Vegas, NV Onsite Hours/Schedule : 40 hours Type ... study participants. * Assist with informed consent and enrollment of study participants in ...

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Clinical Study Assistant information

See Nevada salary details

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$29

How much do clinical study assistant jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for clinical study assistant in Nevada is $20.60, according to ZipRecruiter salary data. Most workers in this role earn between $16.88 and $23.75 per hour, depending on experience, location, and employer.

What is a clinical study assistant?

Clinical Study Assistants are professionals who support the conduct of clinical trials by handling administrative tasks, maintaining study documentation, and ensuring regulatory compliance. They work closely with clinical research teams to coordinate schedules, communicate with study sites, and help manage trial materials. Their role is crucial in ensuring that clinical studies run smoothly, efficiently, and according to protocols and regulatory guidelines.

What are the key skills and qualifications needed to thrive as a clinical study assistant?

To thrive as a Clinical Study Assistant, you need strong organizational skills, attention to detail, and a background in life sciences or related fields, often supported by a bachelor's degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and regulatory documentation processes is typically required. Effective communication, teamwork, and problem-solving skills help you navigate complex study protocols and collaborate with diverse stakeholders. These abilities are crucial for ensuring the accuracy, compliance, and smooth operation of clinical research studies.

What are the main challenges a clinical study assistant might face when supporting clinical trial operations?

A Clinical Study Assistant often encounters challenges such as managing multiple tasks under tight deadlines, ensuring accurate documentation, and coordinating communication between research teams, sponsors, and regulatory bodies. Additionally, adapting to evolving study protocols and maintaining compliance with strict regulatory requirements can be demanding. Strong organizational skills, attention to detail, and proactive communication are essential for navigating these challenges successfully.

What is the difference between Clinical Study Assistant vs Clinical Research Coordinator?

AspectClinical Study AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related fieldUsually requires a bachelor's degree, often with additional certifications in clinical research
Work EnvironmentSupports clinical trials in hospitals, research centers, or pharmaceutical companiesManages entire clinical studies, coordinating between sites, staff, and sponsors
Employer & IndustryHospitals, research institutions, pharmaceutical companiesAcademic medical centers, hospitals, research organizations
Search & Comparison IntentOften compared for entry-level roles supporting clinical trialsCompared for roles with broader responsibilities in clinical study management

The Clinical Study Assistant primarily supports clinical trial activities by assisting with data collection and documentation, while the Clinical Research Coordinator manages the overall conduct of the study, including patient recruitment and compliance. Both roles require similar educational backgrounds but differ in scope and responsibilities within the clinical research process.

What are the most commonly searched types of Clinical Study jobs in Nevada?

The most popular types of Clinical Study jobs in Nevada are:

Infographic showing various Clinical Study Assistant job openings in Nevada as of August 2026, with employment types broken down into 2% As Needed, 80% Full Time, 12% Part Time, and 6% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $42,850 per year, or $20.6 per hour.

Senior Clinical Research Coordinator

Kyvexa Clinical Trials

Las Vegas, NV โ€ข On-site

$25 - $30/hr

Full-time

Posted 16 days ago


Job description

Description
We are seeking an organized, detail-oriented Clinical Research Study Coordinator to join our team. The Study Coordinator will be responsible for the day-to-day management of clinical studies, including subject screening, informed consent, data entry, regulatory compliance, and coordination with investigators and sponsors. This role is ideal for candidates in research who want to grow in a dynamic, fast-paced clinical research environment.
Compensation
  • Pay: $25 - $30 per hour based on experience and performance

Schedule
  • Monday to Friday
  • Full-time

Responsibilities
$44
Qualifications
โ€ข Minimum of 1-2 years of clinical or research experience preferred (medical office or lab experience acceptable).
โ€ข Knowledge of GCP, FDA, and ICH guidelines.
โ€ข Strong organizational, multitasking, and time-management skills.
โ€ข Excellent interpersonal and communication skills (bilingual English/Spanish preferred).
โ€ข Computer proficiency with Microsoft Office and EDC systems.
โ€ข Current CPR, Medical Assistant, and Phlebotomist certifications.