Senior Clinical Research Coordinator
Las Vegas, NV · On-site
$25 - $30/hr
... Research Study Coordinator to join our team ... The Study Coordinator will be responsible for the day-to-day management of clinical studies ...
New
Senior Clinical Research Coordinator
Las Vegas, NV · On-site
$25 - $30/hr
... Research Study Coordinator to join our team ... The Study Coordinator will be responsible for the day-to-day management of clinical studies ...
New
Clinical Research Coordinator Location: Las Vegas, NV Schedule: Monday-Friday | 8:00 AM - 5:00 PM ... Strong organizational skills with the ability to manage multiple priorities and meet deadlines.
Quick apply
Clinical Research Coordinator Location: Las Vegas, NV Schedule: Monday-Friday | 8:00 AM - 5:00 PM ... Strong organizational skills with the ability to manage multiple priorities and meet deadlines.
Health Informatics Manager
Reno, NV · On-site
$48.91 - $60.15/hr
You'll set the informatics roadmap and connect clinical, administrative, and technical partners so ... management, and manage vendors and informatics projects. Required qualifications: - 8 years ...
Health Informatics Manager
Reno, NV · On-site
$48.91 - $60.15/hr
You'll set the informatics roadmap and connect clinical, administrative, and technical partners so ... management, and manage vendors and informatics projects. Required qualifications: - 8 years ...
Clinical Research | Vegas, Nevada
Las Vegas, NV · On-site
$20 - $36/hr
Study Coordination & Participant Management * Screens, recruits, and enrolls eligible oncology ... High School Diploma/GED * 2+ years of clinical research experience, preferably in oncology * 1+ ...
Clinical Research | Vegas, Nevada
Las Vegas, NV · On-site
$20 - $36/hr
Study Coordination & Participant Management * Screens, recruits, and enrolls eligible oncology ... High School Diploma/GED * 2+ years of clinical research experience, preferably in oncology * 1+ ...
Clinical Research | Vegas, Nevada
Las Vegas, NV · On-site
$20 - $36/hr
Study Coordination & Participant Management * Screens, recruits, and enrolls eligible oncology ... High School Diploma/GED * 2+ years of clinical research experience, preferably in oncology * 1+ ...
New
Clinical Research | Vegas, Nevada
Las Vegas, NV · On-site
$20 - $36/hr
Study Coordination & Participant Management * Screens, recruits, and enrolls eligible oncology ... High School Diploma/GED * 2+ years of clinical research experience, preferably in oncology * 1+ ...
New
Clinical Research | Vegas, Nevada
Las Vegas, NV · On-site
$20 - $36/hr
Study Coordination & Participant Management * Screens, recruits, and enrolls eligible oncology ... High School Diploma/GED * 2+ years of clinical research experience, preferably in oncology * 1+ ...
Clinical Research | Vegas, Nevada
Las Vegas, NV · On-site
$20 - $36/hr
Study Coordination & Participant Management * Screens, recruits, and enrolls eligible oncology ... High School Diploma/GED * 2+ years of clinical research experience, preferably in oncology * 1+ ...
Clinical Research | Vegas, Nevada
Las Vegas, NV · On-site
$20 - $36/hr
Study Coordination & Participant Management * Screens, recruits, and enrolls eligible oncology ... High School Diploma/GED * 2+ years of clinical research experience, preferably in oncology * 1+ ...
Clinical Research | Vegas, Nevada
Las Vegas, NV · On-site
$20 - $36/hr
Study Coordination & Participant Management * Screens, recruits, and enrolls eligible oncology ... High School Diploma/GED * 2+ years of clinical research experience, preferably in oncology * 1+ ...
CCCN develops and conducts more than 170 Phase I, Phase II, and Phase III clinical research trials ... Must have excellent communication, time management, and organizational skills, and a strong ability ...
CCCN develops and conducts more than 170 Phase I, Phase II, and Phase III clinical research trials ... Must have excellent communication, time management, and organizational skills, and a strong ability ...
Must have excellent communication, time management, and organizational skills, and a strong ability ... Three years of clinical research experience preferred * Experience in Microsoft Office required
Must have excellent communication, time management, and organizational skills, and a strong ability ... Three years of clinical research experience preferred * Experience in Microsoft Office required
Clinical Research | Vegas, Nevada
Las Vegas, NV · On-site
$20 - $36/hr
... Management * Screens, recruits, and enrolls eligible oncology patients into clinical trials ... Reviews study protocols and prepare study workflows with the research team * Coordinates specimen ...
Clinical Research | Vegas, Nevada
Las Vegas, NV · On-site
$20 - $36/hr
... Management * Screens, recruits, and enrolls eligible oncology patients into clinical trials ... Reviews study protocols and prepare study workflows with the research team * Coordinates specimen ...
Senior Clinical Informatics Analyst (Reno, NV)
Reno, NV · On-site
$80K - $115K/yr
The Senior Clinical Informatics Analyst serves as a strategic partner to hospital C-suite ... Lead change management and user adoption for new or optimized clinical workflows by developing ...
New
Quick apply
Senior Clinical Informatics Analyst (Reno, NV)
Reno, NV · On-site
$80K - $115K/yr
The Senior Clinical Informatics Analyst serves as a strategic partner to hospital C-suite ... Lead change management and user adoption for new or optimized clinical workflows by developing ...
New
Sub Investigator (NP or PA-C)
Las Vegas, NV · On-site
$95K - $129K/yr
Essential Duties and Responsibilities: * Assist the Principal Investigator in the design, implementation, and management of clinical research protocols. * Conduct patient assessments, including ...
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Sub Investigator (NP or PA-C)
Las Vegas, NV · On-site
$95K - $129K/yr
Essential Duties and Responsibilities: * Assist the Principal Investigator in the design, implementation, and management of clinical research protocols. * Conduct patient assessments, including ...
... research and access to no-cost partner resources and education services. Here, you will work ... The RN Manager of Clinical Operations has the rewarding opportunity to travel throughout Nevada ...
... research and access to no-cost partner resources and education services. Here, you will work ... The RN Manager of Clinical Operations has the rewarding opportunity to travel throughout Nevada ...
$14.75 - $19.50/hr
... in clinical research, primarily the Clinical Trial Management System (CTMS). How You'll Create ... Pursuing a bachelor's degree in Computer Science, Information Systems, Health Informatics, Data ...
$14.75 - $19.50/hr
... in clinical research, primarily the Clinical Trial Management System (CTMS). How You'll Create ... Pursuing a bachelor's degree in Computer Science, Information Systems, Health Informatics, Data ...
2025 Fall Intern, Clinical Applications
Sparks, NV · On-site
$15.25 - $20.50/hr
... in clinical research, primarily the Clinical Trial Management System (CTMS). How You'll Create ... Pursuing a bachelor's degree in Computer Science, Information Systems, Health Informatics, Data ...
2025 Fall Intern, Clinical Applications
Sparks, NV · On-site
$15.25 - $20.50/hr
... in clinical research, primarily the Clinical Trial Management System (CTMS). How You'll Create ... Pursuing a bachelor's degree in Computer Science, Information Systems, Health Informatics, Data ...
$15.25 - $20.50/hr
... in clinical research, primarily the Clinical Trial Management System (CTMS). How You'll Create ... Pursuing a bachelor's degree in Computer Science, Information Systems, Health Informatics, Data ...
$15.25 - $20.50/hr
... in clinical research, primarily the Clinical Trial Management System (CTMS). How You'll Create ... Pursuing a bachelor's degree in Computer Science, Information Systems, Health Informatics, Data ...
2025 Fall Intern, Clinical Applications
Henderson, NV · On-site
$13.75 - $18.25/hr
... in clinical research, primarily the Clinical Trial Management System (CTMS). How You'll Create ... Pursuing a bachelor's degree in Computer Science, Information Systems, Health Informatics, Data ...
2025 Fall Intern, Clinical Applications
Henderson, NV · On-site
$13.75 - $18.25/hr
... in clinical research, primarily the Clinical Trial Management System (CTMS). How You'll Create ... Pursuing a bachelor's degree in Computer Science, Information Systems, Health Informatics, Data ...
$14.25 - $19/hr
... in clinical research, primarily the Clinical Trial Management System (CTMS). How You'll Create ... Pursuing a bachelor's degree in Computer Science, Information Systems, Health Informatics, Data ...
$14.25 - $19/hr
... in clinical research, primarily the Clinical Trial Management System (CTMS). How You'll Create ... Pursuing a bachelor's degree in Computer Science, Information Systems, Health Informatics, Data ...
2025 Fall Intern, Clinical Applications
Las Vegas, NV · On-site
$14.25 - $19/hr
... in clinical research, primarily the Clinical Trial Management System (CTMS). How You'll Create ... Pursuing a bachelor's degree in Computer Science, Information Systems, Health Informatics, Data ...
2025 Fall Intern, Clinical Applications
Las Vegas, NV · On-site
$14.25 - $19/hr
... in clinical research, primarily the Clinical Trial Management System (CTMS). How You'll Create ... Pursuing a bachelor's degree in Computer Science, Information Systems, Health Informatics, Data ...
$14 - $18.75/hr
... in clinical research, primarily the Clinical Trial Management System (CTMS). How You'll Create ... Pursuing a bachelor's degree in Computer Science, Information Systems, Health Informatics, Data ...
$14 - $18.75/hr
... in clinical research, primarily the Clinical Trial Management System (CTMS). How You'll Create ... Pursuing a bachelor's degree in Computer Science, Information Systems, Health Informatics, Data ...
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$25 - $30/hr
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Posted 3 days ago
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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
- 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
- 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.
$25 - $30/hour
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.