Irvine Clinical Research, a research site specializing in late phase CNS clinical trials, is seeking applicants for a Clinical Scientist in our enrollment core. The clinical scientist will work on ...
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Irvine Clinical Research, a research site specializing in late phase CNS clinical trials, is seeking applicants for a Clinical Scientist in our enrollment core. The clinical scientist will work on ...
Quick apply
Irvine Clinical Research, a research site specializing in late phase CNS clinical trials, is seeking applicants for a Clinical Scientist in our enrollment core. The clinical scientist will work on ...
Irvine Clinical Research, a research site specializing in late phase CNS clinical trials, is seeking applicants for a Clinical Scientist in our enrollment core. The clinical scientist will work on ...
Quick apply
Irvine Clinical Research, a research site specializing in late phase CNS clinical trials, is seeking applicants for a Clinical Scientist in our enrollment core. The clinical scientist will work on ...
Irvine, CA · On-site
$85K/yr
Irvine Clinical Research, a research site specializing in late phase CNS clinical trials, is seeking applicants for a Clinical Scientist in our enrollment core. The clinical scientist will work on ...
Irvine, CA · On-site
$85K/yr
Irvine Clinical Research, a research site specializing in late phase CNS clinical trials, is seeking applicants for a Clinical Scientist in our enrollment core. The clinical scientist will work on ...
Riverside, CA · On-site
$85K/yr
Irvine Clinical Research, a research site specializing in late phase CNS clinical trials, is seeking applicants for a Clinical Scientist in our enrollment core. The clinical scientist will work on ...
Riverside, CA · On-site
$85K/yr
Irvine Clinical Research, a research site specializing in late phase CNS clinical trials, is seeking applicants for a Clinical Scientist in our enrollment core. The clinical scientist will work on ...
Irvine, CA · On-site
Reporting to the Senior Manager, Clinical Safety, the Specialist, Clinical Safety supports the conduct and timely execution of JenaValve clinical trials by monitoring subject safety, ensuring ...
Irvine, CA · On-site
Reporting to the Senior Manager, Clinical Safety, the Specialist, Clinical Safety supports the conduct and timely execution of JenaValve clinical trials by monitoring subject safety, ensuring ...
Irvine, CA · On-site
$100K/yr
Reporting to the Senior Manager, Clinical Safety, the Specialist, Clinical Safety supports the conduct and timely execution of JenaValve clinical trials by monitoring subject safety, ensuring ...
Irvine, CA · On-site
$100K/yr
Reporting to the Senior Manager, Clinical Safety, the Specialist, Clinical Safety supports the conduct and timely execution of JenaValve clinical trials by monitoring subject safety, ensuring ...
Irvine, CA · On-site
Reporting to the Senior Manager, Clinical Safety, the Specialist, Clinical Safety supports the conduct and timely execution of JenaValve clinical trials by monitoring subject safety, ensuring ...
Irvine, CA · On-site
Reporting to the Senior Manager, Clinical Safety, the Specialist, Clinical Safety supports the conduct and timely execution of JenaValve clinical trials by monitoring subject safety, ensuring ...
Irvine, CA · On-site
Reporting to the Senior Manager, Clinical Safety, the Specialist, Clinical Safety supports the conduct and timely execution of JenaValve clinical trials by monitoring subject safety, ensuring ...
Irvine, CA · On-site
Reporting to the Senior Manager, Clinical Safety, the Specialist, Clinical Safety supports the conduct and timely execution of JenaValve clinical trials by monitoring subject safety, ensuring ...
Irvine, CA · On-site
$30 - $40/hr
As a Research Dietitian / Coordinator, you will play a crucial role in these clinical trials. In this hybrid role, you will be expected to counsel study participants on lifestyle measures while ...
Irvine, CA · On-site
$30 - $40/hr
As a Research Dietitian / Coordinator, you will play a crucial role in these clinical trials. In this hybrid role, you will be expected to counsel study participants on lifestyle measures while ...
Riverside, CA · On-site
$30 - $40/hr
As a Research Dietitian / Coordinator, you will play a crucial role in these clinical trials. In this hybrid role, you will be expected to counsel study participants on lifestyle measures while ...
Quick apply
Riverside, CA · On-site
$30 - $40/hr
As a Research Dietitian / Coordinator, you will play a crucial role in these clinical trials. In this hybrid role, you will be expected to counsel study participants on lifestyle measures while ...
Riverside, CA · On-site
$30 - $40/hr
As a Research Dietitian / Coordinator, you will play a crucial role in these clinical trials. In this hybrid role, you will be expected to counsel study participants on lifestyle measures while ...
Riverside, CA · On-site
$30 - $40/hr
As a Research Dietitian / Coordinator, you will play a crucial role in these clinical trials. In this hybrid role, you will be expected to counsel study participants on lifestyle measures while ...
Irvine, CA · On-site
$30 - $40/hr
As a Research Dietitian / Coordinator, you will play a crucial role in these clinical trials. In this hybrid role, you will be expected to counsel study participants on lifestyle measures while ...
Quick apply
Irvine, CA · On-site
$30 - $40/hr
As a Research Dietitian / Coordinator, you will play a crucial role in these clinical trials. In this hybrid role, you will be expected to counsel study participants on lifestyle measures while ...
Irvine, CA · On-site
$18 - $32/hr
The Medical Assistant will be responsible for assisting the Research Study Coordinator in recruiting subjects for assigned clinical trials and coordinating the research activities and visits for the ...
Quick apply
Irvine, CA · On-site
$18 - $32/hr
The Medical Assistant will be responsible for assisting the Research Study Coordinator in recruiting subjects for assigned clinical trials and coordinating the research activities and visits for the ...
Irvine, CA · On-site
$18 - $32/hr
The Medical Assistant will be responsible for assisting the Research Study Coordinator in recruiting subjects for assigned clinical trials and coordinating the research activities and visits for the ...
Quick apply
Irvine, CA · On-site
$18 - $32/hr
The Medical Assistant will be responsible for assisting the Research Study Coordinator in recruiting subjects for assigned clinical trials and coordinating the research activities and visits for the ...
Irvine, CA · On-site
$18 - $32/hr
The Medical Assistant will be responsible for assisting the Research Study Coordinator in recruiting subjects for assigned clinical trials and coordinating the research activities and visits for the ...
Quick apply
Irvine, CA · On-site
$18 - $32/hr
The Medical Assistant will be responsible for assisting the Research Study Coordinator in recruiting subjects for assigned clinical trials and coordinating the research activities and visits for the ...
Riverside, CA · On-site
$30 - $40/hr
As a Research Dietitian / Coordinator, you will play a crucial role in these clinical trials. In this hybrid role, you will be expected to counsel study participants on lifestyle measures while ...
Riverside, CA · On-site
$30 - $40/hr
As a Research Dietitian / Coordinator, you will play a crucial role in these clinical trials. In this hybrid role, you will be expected to counsel study participants on lifestyle measures while ...
Irvine, CA · On-site
$30 - $40/hr
As a Research Dietitian / Coordinator, you will play a crucial role in these clinical trials. In this hybrid role, you will be expected to counsel study participants on lifestyle measures while ...
Irvine, CA · On-site
$30 - $40/hr
As a Research Dietitian / Coordinator, you will play a crucial role in these clinical trials. In this hybrid role, you will be expected to counsel study participants on lifestyle measures while ...
Reporting to the Senior Director of Clinical Affairs, the Manager, Clinical Affairs (CRB) will be responsible for case planning for global clinical trials and collaborating with internal and external ...
Reporting to the Senior Director of Clinical Affairs, the Manager, Clinical Affairs (CRB) will be responsible for case planning for global clinical trials and collaborating with internal and external ...
Irvine, CA · On-site +1
$145K/yr
Reporting to the Senior Director of Clinical Affairs, the Manager, Clinical Affairs (CRB) will be responsible for case planning for global clinical trials and collaborating with internal and external ...
Irvine, CA · On-site +1
$145K/yr
Reporting to the Senior Director of Clinical Affairs, the Manager, Clinical Affairs (CRB) will be responsible for case planning for global clinical trials and collaborating with internal and external ...
Oversee the planning, initiation, and execution of clinical trials at the site * Maintains required records of study activity including case report forms, drug dispensation records, and regulatory ...
Oversee the planning, initiation, and execution of clinical trials at the site * Maintains required records of study activity including case report forms, drug dispensation records, and regulatory ...
$30.09 - $36.48
4% of jobs
$36.48 - $42.86
6% of jobs
$42.86 - $49.25
7% of jobs
$54.03 is the 25th percentile. Wages below this are outliers.
$49.25 - $55.63
9% of jobs
$55.63 - $62.01
15% of jobs
The median wage is $64.83 / hr.
$62.01 - $68.40
18% of jobs
$72.94 is the 75th percentile. Wages above this are outliers.
$68.40 - $74.78
21% of jobs
$74.78 - $81.16
7% of jobs
$81.16 - $87.55
6% of jobs
$87.55 - $93.93
3% of jobs
$93.93 - $100.31
2% of jobs
$30
$65
$100
A Clinical Trials job involves managing, coordinating, or supporting research studies that evaluate the safety and effectiveness of medical treatments, drugs, or devices. Professionals in this field work on trial design, patient recruitment, data collection, regulatory compliance, and reporting results. Roles can range from clinical research coordinators to trial managers and regulatory specialists. The goal is to ensure that studies follow ethical guidelines and produce reliable data for medical advancements.
Many professionals in Clinical Trials start their careers as Clinical Research Coordinators, Clinical Research Associates, or Data Managers. With experience, you can advance to roles such as Senior Clinical Research Associate, Clinical Trial Manager, or Project Manager, and potentially move into areas like regulatory affairs, medical writing, or quality assurance. The role offers continuous learning opportunities, exposure to innovative therapies, and often provides the chance to lead larger, more complex studies as you progress. Advancement is typically supported by additional certifications, strong performance, and a proactive approach to professional development. Teamwork and networking within the industry can also open new doors for growth.
To thrive in Clinical Trials roles, you need a strong understanding of clinical research principles, Good Clinical Practice (GCP) guidelines, and a background in life sciences or healthcare. Familiarity with electronic data capture (EDC) systems, regulatory compliance software, and relevant certifications such as GCP or CCRA is highly valuable. Attention to detail, organizational skills, and effective communication enable collaboration across multidisciplinary teams. These competencies are crucial for ensuring protocol adherence, data integrity, and the successful execution of trial activities.
The most popular types of Clinical Trials jobs in Riverside, CA are:
For Clinical Trials jobs in Riverside, CA, the most frequently searched job titles are:
The top searched job categories for Clinical Trials jobs in Riverside, CA are:
Cities near Riverside, CA with the most Clinical Trials job openings:

$85K/yr
Full-time
Re-posted 14 days ago