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Senior Clinical Research Rater Jobs in Nevada (NOW HIRING)

System One

Clinical Research Coordinator

Las Vegas, NV · On-site

$23.25 - $30.75/hr

Contract Responsibilities * Assist in the coordination and execution of clinical research protocols under the supervision of the PI and senior research staff. * Conduct screening visits to collect ...

System One

Clinical Research Coordinator

Las Vegas, NV · On-site

$23.25 - $30.75/hr

Contract Responsibilities * Assist in the coordination and execution of clinical research protocols under the supervision of the PI and senior research staff. * Conduct screening visits to collect ...

System One

Clinical Research Coordinator

Las Vegas, NV · On-site

$23.25 - $30.75/hr

Contract Responsibilities * Assist in the coordination and execution of clinical research protocols under the supervision of the PI and senior research staff. * Conduct screening visits to collect ...

System One

Clinical Research Coordinator

Las Vegas, NV · On-site

$23.25 - $30.75/hr

Contract Responsibilities * Assist in the coordination and execution of clinical research protocols under the supervision of the PI and senior research staff. * Conduct screening visits to collect ...

System One

Clinical Research Coordinator

Las Vegas, NV · On-site

$23.25 - $30.75/hr

Contract Responsibilities * Assist in the coordination and execution of clinical research protocols under the supervision of the PI and senior research staff. * Conduct screening visits to collect ...

IQVIA

Clinical Trial Psych Rater

Las Vegas, NV · Remote

$62K - $156K/yr

Clinical Trial Psych Rater - US Spanish Speaking Location: Remote/Virtual Hours: Estimated 10-16 ... Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral ...

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Senior Clinical Research Rater information

What is the difference between Senior Clinical Research Rater vs Clinical Research Coordinator?

AspectSenior Clinical Research RaterClinical Research Coordinator
Required CredentialsTypically requires a background in healthcare, psychology, or related fields; certifications like CCRP are commonOften requires a degree in health sciences, nursing, or related fields; certifications like CCRP or CRC are beneficial
Work EnvironmentPrimarily conducts assessments, reviews data, and supports clinical trials remotely or in research settingsManages trial logistics, coordinates with sites, and oversees study activities in clinical settings
Employer & Industry UsageUsed by pharmaceutical companies, research organizations, and CROs for patient assessmentsEmployed by hospitals, research institutions, and CROs to manage trial operations

The main difference is that Senior Clinical Research Raters focus on evaluating patient data and assessments, often remotely, while Clinical Research Coordinators handle the overall management and coordination of clinical trials on-site. Both roles require healthcare or research backgrounds but serve different functions within the clinical research process.

Senior Clinical Research Rater jobs near you

Senior Clinical Research Coordinator

Kyvexa Trials

Las Vegas, NV • On-site

$25 - $30/hr

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Posted yesterday

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Job description

Description

Position Summary

We are seeking an organized, detail-oriented Senior 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


  • Coordinate and conduct clinical trials according to GCP, ICH, FDA, and sponsor guidelines.
  • Recruit, screen, and enroll eligible study participants.
  • Obtain and document informed consent from subjects.
  • Perform study-related procedures such as specimen collection, vitals, or device use per protocol.
  • Schedule and manage subject visits, ensuring protocol adherence and accurate source documentation.
  • Enter data into Electronic Data Capture (EDC) systems and maintain study binders.
  • Maintain regulatory files, site logs, and documentation readiness for audits or monitoring visits.
  • Communicate with sponsors, CROs, monitors, and physicians regarding study progress and data queries.
  • Ensure subject confidentiality and compliance with HIPAA.
  • Assist in IRB submissions, amendments, and ongoing study correspondence.
  • Traveling required from Kyvexa headquarters to clinics around the Las Vegas Valley and vice versa
Qualifications
  • Minimum 1–2 years of clinical or research experience preferred (medical office or lab experience acceptable).
  • Knowledge of GCP, FDA, and ICH guidelines.
  • Strong organizational, multitasking, and time-management skills.
  • Excellent interpersonal and communication skills (bilingual English/Spanish preferred).
  • Computer proficiency with Microsoft Office and EDC systems.
  • Current CPR, Medical Assistant, and Phlebotomist certifications.
Compensation

$25 - $30/hour

About Kyvexa Trials

Kyvexa partners with sponsors and investigators to deliver reliable, patient-centered clinical trial site management for medical device research — combining regulatory rigor, operational excellence, and compassionate care to help bring safe, effective devices to market faster. At Kyvexa, we exist to make medical device clinical trials safer and more human — supporting patients, physicians, and sponsors with the highest standards of care, compliance, and integrity.



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