Clinical Research Coordinator
$31 - $38/hr
The Clinical Research Coordinator assists the Investigators in executing Phase I, II, III, and IV ... Document assessments and study data per regs/GCP; maintain complete source; accurately complete ...
$31 - $38/hr
The Clinical Research Coordinator assists the Investigators in executing Phase I, II, III, and IV ... Document assessments and study data per regs/GCP; maintain complete source; accurately complete ...
$31 - $38/hr
The Clinical Research Coordinator assists the Investigators in executing Phase I, II, III, and IV ... Document assessments and study data per regs/GCP; maintain complete source; accurately complete ...
Murrieta, CA · On-site
$31 - $38/hr
The Clinical Research Coordinator assists the Investigators in executing Phase I, II, III, and IV ... Document assessments and study data per regs/GCP; maintain complete source; accurately complete ...
Murrieta, CA · On-site
$31 - $38/hr
The Clinical Research Coordinator assists the Investigators in executing Phase I, II, III, and IV ... Document assessments and study data per regs/GCP; maintain complete source; accurately complete ...
Murrieta, CA · On-site
$31 - $38/hr
The Clinical Research Coordinator assists the Investigators in executing Phase I, II, III, and IV ... Document assessments and study data per regs/GCP; maintain complete source; accurately complete ...
Quick apply
Murrieta, CA · On-site
$31 - $38/hr
The Clinical Research Coordinator assists the Investigators in executing Phase I, II, III, and IV ... Document assessments and study data per regs/GCP; maintain complete source; accurately complete ...
Communicate with investigators, coordinators, and study teams about participants * Assist with ... clinical trials. This is a full-time employment position based in-person at one of our clinics. The ...
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Communicate with investigators, coordinators, and study teams about participants * Assist with ... clinical trials. This is a full-time employment position based in-person at one of our clinics. The ...
Riverside, CA · On-site
$85K/yr
Communicate with investigators, coordinators, and study teams about participants * Assist with ... clinical trials. This is a full-time employment position based in-person at one of our clinics. The ...
Quick apply
Riverside, CA · On-site
$85K/yr
Communicate with investigators, coordinators, and study teams about participants * Assist with ... clinical trials. This is a full-time employment position based in-person at one of our clinics. The ...
Communicate with investigators, coordinators, and study teams about participants * Assist with ... clinical trials. This is a full-time employment position based in-person at one of our clinics. The ...
Communicate with investigators, coordinators, and study teams about participants * Assist with ... clinical trials. This is a full-time employment position based in-person at one of our clinics. The ...
Riverside, CA · On-site
$85K/yr
Communicate with investigators, coordinators, and study teams about participants * Assist with ... clinical trials. This is a full-time employment position based in-person at one of our clinics. The ...
Riverside, CA · On-site
$85K/yr
Communicate with investigators, coordinators, and study teams about participants * Assist with ... clinical trials. This is a full-time employment position based in-person at one of our clinics. The ...
Riverside, CA · On-site
$125K - $130K/yr
... study coordinators Job Requirements * Valid license to practice in California as an NP or PA-C, free and unencumbered * Experience working with older adults in a clinical or research setting
Riverside, CA · On-site
$125K - $130K/yr
... study coordinators Job Requirements * Valid license to practice in California as an NP or PA-C, free and unencumbered * Experience working with older adults in a clinical or research setting
Riverside, CA · On-site
$125K - $130K/yr
... study coordinators Job Requirements * Valid license to practice in California as an NP or PA-C, free and unencumbered * Experience working with older adults in a clinical or research setting
Riverside, CA · On-site
$125K - $130K/yr
... study coordinators Job Requirements * Valid license to practice in California as an NP or PA-C, free and unencumbered * Experience working with older adults in a clinical or research setting
$300K - $350K/yr
Conduct clinical intake interviews to determine medical eligibility of potential study participants ... Provide medical leadership to our team of psychologists and study coordinators Job Requirements
$300K - $350K/yr
Conduct clinical intake interviews to determine medical eligibility of potential study participants ... Provide medical leadership to our team of psychologists and study coordinators Job Requirements
Conduct clinical intake interviews to determine medical eligibility of potential study participants ... Provide medical leadership to our team of psychologists and study coordinators Job Requirements
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Conduct clinical intake interviews to determine medical eligibility of potential study participants ... Provide medical leadership to our team of psychologists and study coordinators Job Requirements
Irvine, CA · On-site
$300K - $350K/yr
Conduct clinical intake interviews to determine medical eligibility of potential study participants ... Provide medical leadership to our team of psychologists and study coordinators Job Requirements
Irvine, CA · On-site
$300K - $350K/yr
Conduct clinical intake interviews to determine medical eligibility of potential study participants ... Provide medical leadership to our team of psychologists and study coordinators Job Requirements
Riverside, CA · On-site
$300K/yr
Conduct clinical intake interviews to determine medical eligibility of potential study participants ... Provide medical leadership to our team of psychologists and study coordinators Job Requirements
Quick apply
Riverside, CA · On-site
$300K/yr
Conduct clinical intake interviews to determine medical eligibility of potential study participants ... Provide medical leadership to our team of psychologists and study coordinators Job Requirements
Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor ... Gains an in-depth understanding of the study protocol and related procedures.Coordinates & manages ...
Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor ... Gains an in-depth understanding of the study protocol and related procedures.Coordinates & manages ...
Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor ... Gains an in-depth understanding of the study protocol and related procedures. * Coordinates ...
Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor ... Gains an in-depth understanding of the study protocol and related procedures. * Coordinates ...
... study coordinators Job Requirements * Valid license to practice in California as an NP or PA-C, free and unencumbered * Experience working with older adults in a clinical or research setting
Quick apply
... study coordinators Job Requirements * Valid license to practice in California as an NP or PA-C, free and unencumbered * Experience working with older adults in a clinical or research setting
Irvine, CA · On-site
$140K/yr
... study coordinators Job Requirements * Valid license to practice in California as an NP or PA-C, free and unencumbered * Experience working with older adults in a clinical or research setting
Irvine, CA · On-site
$140K/yr
... study coordinators Job Requirements * Valid license to practice in California as an NP or PA-C, free and unencumbered * Experience working with older adults in a clinical or research setting
... study coordinators Job Requirements * Valid license to practice in California as an NP or PA-C, free and unencumbered * Experience working with older adults in a clinical or research setting
... study coordinators Job Requirements * Valid license to practice in California as an NP or PA-C, free and unencumbered * Experience working with older adults in a clinical or research setting
Murrieta, CA · On-site
$31 - $38/hr
Document assessments and study data per regs/GCP; maintain complete source; accurately complete ... Must have oncology clinical research experience * Minimum of two years of clinical research ...
Murrieta, CA · On-site
$31 - $38/hr
Document assessments and study data per regs/GCP; maintain complete source; accurately complete ... Must have oncology clinical research experience * Minimum of two years of clinical research ...
Irvine, CA · On-site
$100K/yr
... coordinating a large portfolio of complex oncology clinical studies, and is responsible for staff performance management, and programmatic workflow of projects. Supervises and delegates staff ...
Irvine, CA · On-site
$100K/yr
... coordinating a large portfolio of complex oncology clinical studies, and is responsible for staff performance management, and programmatic workflow of projects. Supervises and delegates staff ...
$29.2K - $37.6K
3% of jobs
$37.6K - $45.9K
7% of jobs
$45.9K - $54.2K
11% of jobs
$55.5K is the 25th percentile. Wages below this are outliers.
$54.2K - $62.6K
26% of jobs
The median wage is $63.8K / yr.
$62.6K - $70.9K
21% of jobs
$77.7K is the 75th percentile. Wages above this are outliers.
$70.9K - $79.3K
9% of jobs
$79.3K - $87.6K
10% of jobs
$87.6K - $96K
6% of jobs
$96K - $104.3K
6% of jobs
$104.3K - $112.7K
1% of jobs
$112.7K - $121K
0% of jobs
$29.2K
$70.5K
$121K
| Aspect | Clinical Study Coordinator | Clinical Research Associate |
|---|---|---|
| Required Credentials | Typically a bachelor's degree in health sciences or related field; certifications like CCRP are a plus | Often a bachelor's degree in life sciences; certifications like CCRP or RAC are common |
| Work Environment | Conducts site visits, manages study activities at clinical sites | Monitors multiple sites remotely or on-site, ensuring protocol compliance |
| Employer & Industry Usage | Hospitals, clinics, research sites | Pharmaceutical companies, CROs, biotech firms |
While both roles support clinical research, Clinical Study Coordinators focus on managing day-to-day site activities, whereas Clinical Research Associates primarily monitor and oversee multiple sites to ensure regulatory compliance and data integrity.
The most popular types of Clinical Study jobs in Riverside, CA are:
The top searched job categories for Clinical Study Coordinator jobs in Riverside, CA are:
Cities near Riverside, CA with the most Clinical Study Coordinator job openings:

$31 - $38/hr
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted 21 days ago
Valkyrie Clinical Trials, a Flourish Research company, is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives! We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities.
We are actively hiring Clinical Research Coordinators at our Murrieta site location.
The Clinical Research Coordinator assists the Investigators in executing Phase I, II, III, and IV clinical research trials in accordance with Standard Operating Procedures (SOPs), FDA and GCP guidelines, and study protocols while providing an impeccable patient experience in every, single interaction.
Shift: Monday-Friday, 8:30 AM - 5 PM (occasional weekends)
Location: 25405 Hancock Ave, Suite 110, Murrieta, CA 92562
Compensation: $31.00-$38.00/hr depending on experience
RESPONSIBILITIES
Requirements
Flourish Research offers an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities. Apply today to learn more about how you can join us in our mission to save and improve the lives of others!
Benefits
Health, dental, and vision insurance plans, 401(k) with a 100% employer match on the first 4% of employee contributions, tuition reimbursement, parental leave, referral program, employee assistance program, life insurance, disability insurance, and 15 days of PTO + 8 paid holidays and 2 floating holidays.
Flourish Research is where clinical trials thrive.
Flourish Research is one of the industry's most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research.
At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality.
Flourish Research is driven by a diverse and inclusive community of passionate people who are committed to improving the quality of life of communities around the world. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect.
Flourish Research strives to build an organization that attracts and leverages diversity in our staff, which reflects the diversity of our local communities. We promote education, acceptance, and inclusion because there is beauty in diversity. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU!
Flourish Research is an equal employment opportunity employer. Employment decisions are based on merit and business needs, and not on race, color, sex, (including pregnancy and gender identity), citizenship status, national origin, ancestry, gender, sexual orientation, age, religion, creed, physical or mental disability, genetic information, marital status, veteran status, political affiliation, or any other factor protected by law. Flourish Research complies with the law regarding reasonable accommodation for handicapped and disabled employees.
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Pharmaceutical and medicine manufacturing
201 - 500 Employees
New York, NY, US
2021