The position works directly with physicians, investigators, research coordinators, patients, and internal partners to support clinical study execution, device-related procedures, programming ...
The position works directly with physicians, investigators, research coordinators, patients, and internal partners to support clinical study execution, device-related procedures, programming ...
Principal Field Technical Service Specialist - NMPH - Remote within USA (Open)
Irvine, CA · On-site +1
The position works directly with physicians, investigators, research coordinators, patients, and internal partners to support clinical study execution, device-related procedures, programming ...
Principal Field Technical Service Specialist - NMPH - Remote within USA (Open)
Irvine, CA · On-site +1
The position works directly with physicians, investigators, research coordinators, patients, and internal partners to support clinical study execution, device-related procedures, programming ...
Senior Clinical Research Coordinator
Riverside, CA · On-site
$76K - $90K/yr
The Senior Clinical Research Coordinator manages study conduct from planning through study closeout. Position Type: Full Time Pay Range: $76,000-$90,000/yr Location: Riverside, CA Work Schedule:
Senior Clinical Research Coordinator
Riverside, CA · On-site
$76K - $90K/yr
The Senior Clinical Research Coordinator manages study conduct from planning through study closeout. Position Type: Full Time Pay Range: $76,000-$90,000/yr Location: Riverside, CA Work Schedule:
Collaborate with study coordinators, nurses, and research staff. * Attend protocol-related training sessions and maintain compliance with Good Clinical Practice (GCP). Qualifications: * MD or DO with ...
Collaborate with study coordinators, nurses, and research staff. * Attend protocol-related training sessions and maintain compliance with Good Clinical Practice (GCP). Qualifications: * MD or DO with ...
Clinical Research Coordinator (Experienced) (Bilingual-Spanish) (Riverside)
Riverside, CA · On-site
$66K - $80K/yr
Perform study procedures in accordance with GCP and study protocols * Organize and maintain study ... One (1) or more years of clinical research coordinator experience * Attention to detail and the ...
Clinical Research Coordinator (Experienced) (Bilingual-Spanish) (Riverside)
Riverside, CA · On-site
$66K - $80K/yr
Perform study procedures in accordance with GCP and study protocols * Organize and maintain study ... One (1) or more years of clinical research coordinator experience * Attention to detail and the ...
Clinical Research Coordinator (Experienced) (Bilingual-Spanish) (Riverside)
Riverside, CA · On-site
$66K - $80K/yr
Perform study procedures in accordance with GCP and study protocols * Organize and maintain study ... One (1) or more years of clinical research coordinator experience * Attention to detail and the ...
Clinical Research Coordinator (Experienced) (Bilingual-Spanish) (Riverside)
Riverside, CA · On-site
$66K - $80K/yr
Perform study procedures in accordance with GCP and study protocols * Organize and maintain study ... One (1) or more years of clinical research coordinator experience * Attention to detail and the ...
Clinical Research Coordinator (Experienced) (Bilingual-Spanish) (Riverside)
Riverside, CA · On-site
$66K - $80K/yr
Perform study procedures in accordance with GCP and study protocols * Organize and maintain study ... One (1) or more years of clinical research coordinator experience * Attention to detail and the ...
Quick apply
Clinical Research Coordinator (Experienced) (Bilingual-Spanish) (Riverside)
Riverside, CA · On-site
$66K - $80K/yr
Perform study procedures in accordance with GCP and study protocols * Organize and maintain study ... One (1) or more years of clinical research coordinator experience * Attention to detail and the ...
Manager Clinical Affairs
Irvine, CA · On-site
Coordinates and oversees all clinical trial startup and site closure activities, ensuring that ... Facilitates timely site activation to accelerate study initiation and minimize time to first ...
Manager Clinical Affairs
Irvine, CA · On-site
Coordinates and oversees all clinical trial startup and site closure activities, ensuring that ... Facilitates timely site activation to accelerate study initiation and minimize time to first ...
Manager Clinical Affairs
Irvine, CA · On-site +1
Coordinates and oversees all clinical trial startup and site closure activities, ensuring that ... Facilitates timely site activation to accelerate study initiation and minimize time to first ...
Manager Clinical Affairs
Irvine, CA · On-site +1
Coordinates and oversees all clinical trial startup and site closure activities, ensuring that ... Facilitates timely site activation to accelerate study initiation and minimize time to first ...
Psychiatrist (Clinical Trial Physician) - Tustin, CA
Tustin, CA · On-site
$100 - $200/hr
Collaborate with study coordinators, nurses, and research staff. * Attend protocol-related training sessions and maintain compliance with Good Clinical Practice (GCP). Education, Licensure, and ...
Psychiatrist (Clinical Trial Physician) - Tustin, CA
Tustin, CA · On-site
$100 - $200/hr
Collaborate with study coordinators, nurses, and research staff. * Attend protocol-related training sessions and maintain compliance with Good Clinical Practice (GCP). Education, Licensure, and ...
Executive Medical Director, Immunology Clinical Development - Respiratory/Pulmonary
Irvine, CA · On-site
$234K/yr
Has overall responsibility for leading clinical study teams, monitoring overall study integrity ... area, coordinating and leading appropriate scientific and medical activities with internal ...
Executive Medical Director, Immunology Clinical Development - Respiratory/Pulmonary
Irvine, CA · On-site
$234K/yr
Has overall responsibility for leading clinical study teams, monitoring overall study integrity ... area, coordinating and leading appropriate scientific and medical activities with internal ...
Senior Clinical Research Coordinator
Riverside, CA · On-site
$76K - $90K/yr
The Senior Clinical Research Coordinator manages study conduct from planning through study closeout. Position Type: Full Time Pay Range: $76,000-$90,000/yr Location: Riverside, CA Work Schedule:
Senior Clinical Research Coordinator
Riverside, CA · On-site
$76K - $90K/yr
The Senior Clinical Research Coordinator manages study conduct from planning through study closeout. Position Type: Full Time Pay Range: $76,000-$90,000/yr Location: Riverside, CA Work Schedule:
Manager, Clinical Affairs (Case Review Board)
Irvine, CA · On-site +1
$145K/yr
Oversee the training/coordinating of subject presentation materials for CRB meetings with clinical ... Working knowledge of clinical study execution and patient screen / case planning. * Knowledge of ...
Manager, Clinical Affairs (Case Review Board)
Irvine, CA · On-site +1
$145K/yr
Oversee the training/coordinating of subject presentation materials for CRB meetings with clinical ... Working knowledge of clinical study execution and patient screen / case planning. * Knowledge of ...
Oversee the training/coordinating of subject presentation materials for CRB meetings with clinical ... Working knowledge of clinical study execution and patient screen / case planning. * Knowledge of ...
Oversee the training/coordinating of subject presentation materials for CRB meetings with clinical ... Working knowledge of clinical study execution and patient screen / case planning. * Knowledge of ...
Senior Clinical Research Coordinator
Riverside, CA · On-site
$25.25 - $33.75/hr
Our Riverside site is known for its depth of experience, thoughtful study execution, and team-based ... clinical trial studies as the primary coordinator required * High school diploma or GED required
Senior Clinical Research Coordinator
Riverside, CA · On-site
$25.25 - $33.75/hr
Our Riverside site is known for its depth of experience, thoughtful study execution, and team-based ... clinical trial studies as the primary coordinator required * High school diploma or GED required
Senior Clinical Research Coordinator
Riverside, CA · On-site
$25.25 - $33.75/hr
Our Riverside site is known for its depth of experience, thoughtful study execution, and team-based ... clinical trial studies as the primary coordinator required * High school diploma or GED required
Senior Clinical Research Coordinator
Riverside, CA · On-site
$25.25 - $33.75/hr
Our Riverside site is known for its depth of experience, thoughtful study execution, and team-based ... clinical trial studies as the primary coordinator required * High school diploma or GED required
Project Specialist 2
Santa Ana, CA · On-site
ManagesClinical Supply Chain for J&J Vision clinical studies by forecasting shipment needs, sourcing vendors, and coordinating budget, and sourcing andtracking ofsupplies for study start-up and ...
Project Specialist 2
Santa Ana, CA · On-site
ManagesClinical Supply Chain for J&J Vision clinical studies by forecasting shipment needs, sourcing vendors, and coordinating budget, and sourcing andtracking ofsupplies for study start-up and ...
Senior Clinical Research Coordinator
Riverside, CA · On-site
$85K - $90K/yr
Our Riverside site is known for its depth of experience, thoughtful study execution, and team-based ... clinical trial studies as the primary coordinator required * High school diploma or GED required
Senior Clinical Research Coordinator
Riverside, CA · On-site
$85K - $90K/yr
Our Riverside site is known for its depth of experience, thoughtful study execution, and team-based ... clinical trial studies as the primary coordinator required * High school diploma or GED required
Senior Clinical Research Coordinator
Riverside, CA · On-site
$85K - $90K/yr
Our Riverside site is known for its depth of experience, thoughtful study execution, and team-based ... clinical trial studies as the primary coordinator required * High school diploma or GED required
Senior Clinical Research Coordinator
Riverside, CA · On-site
$85K - $90K/yr
Our Riverside site is known for its depth of experience, thoughtful study execution, and team-based ... clinical trial studies as the primary coordinator required * High school diploma or GED required
Project Specialist 2
Santa Ana, CA · On-site
Manages Clinical Supply Chain for J&J Vision clinical studies by forecasting shipment needs, sourcing vendors, and coordinating budget, and sourcing and tracking of supplies for study start-up and ...
Project Specialist 2
Santa Ana, CA · On-site
Manages Clinical Supply Chain for J&J Vision clinical studies by forecasting shipment needs, sourcing vendors, and coordinating budget, and sourcing and tracking of supplies for study start-up and ...
Clinical Study Coordinator information
See Riverside, CA salary details
$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
How much do clinical study coordinator jobs pay per year?
What are the key skills and qualifications needed to thrive as a clinical study coordinator?
What are some common challenges clinical study coordinators face when managing multiple studies at once?
What is the difference between Clinical Study Coordinator vs Clinical Research Associate?
| 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.
What are the most commonly searched types of Clinical Study jobs in Riverside, CA?
The most popular types of Clinical Study jobs in Riverside, CA are:
What job categories do people searching Clinical Study Coordinator jobs in Riverside, CA look for?
The top searched job categories for Clinical Study Coordinator jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Clinical Study Coordinator jobs?
Cities near Riverside, CA with the most Clinical Study Coordinator job openings:

Principal Field Technical Service Specialist - NMPH - Remote within USA (Open)
Irvine, CA • On-site
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 4 days ago
Medtronic rating
7.9
Based on 180 frontline employees who took The Breakroom Quiz
154th of 545 rated manufacturers
Job description
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first - developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.
A Day in the LifeThe Neuromodulation and Pelvic Health Clinical Research organization partners with physicians, research sites, and cross-functional teams to advance evidence generation and support the safe and effective use of investigational and commercial therapies. This team provides field-based clinical and technical expertise throughout the clinical study lifecycle, helping sites execute study protocols, optimize device utilization, support patient management, and deliver high-quality study outcomes.This is a remote U.S.-based role requiring residence within the assigned region. The position supports clinical research activities across multiple study sites and healthcare settings through a combination of in-person and virtual engagement. Travel is expected approximately 70% to 75% of the time, including air and ground travel, with occasional work across multiple U.S. time zones.
Check us out on LinkedIn: Medtronic Brain Modulation and Pain Interventions
Check us out on LinkedIn: Medtronic Pelvic Health
This field-based clinical research support role serves as a key technical and clinical resource for investigational and commercial Neuromodulation and Pelvic Health therapies. The position works directly with physicians, investigators, research coordinators, patients, and internal partners to support clinical study execution, device-related procedures, programming activities, protocol adherence, patient follow-up, and technical issue resolution. The role also contributes field insights that help improve study design, training strategies, patient experience, and future product development activities.
Primary Responsibilities
Provide field-based technical, procedural, and clinical support for Neuromodulation and Pelvic Health clinical studies, including implant procedures, device programming, follow-up visits, troubleshooting, and study-related patient support.
Partner with physicians, investigators, research coordinators, and site personnel to support protocol compliance, enrollment activities, patient follow-up, and high-quality data collection throughout the study lifecycle.
Serve as a technical resource across Clinical Research, Engineering, Research and Technology, Medical Affairs, and field teams to support effective clinical study execution.
Support study planning, activation, and site initiation activities, including review of clinical investigational plans, workflows, training materials, technical documentation, and site support strategies.
Deliver education and training to physicians, research staff, internal teams, and field personnel on device functionality, therapy delivery, programming, procedural workflows, and study-specific requirements.
Document field observations, technical issues, study execution challenges, and customer feedback; communicate trends and recommendations to appropriate stakeholders.
Collaborate with cross-functional partners to identify study risks, remove execution barriers, and improve operational effectiveness across clinical research programs.
Mentor and provide technical guidance to clinical and field-based colleagues by sharing best practices, workflow knowledge, and study support expertise.
Required Qualifications
High School Diploma or GED and 10+ years; OR Associate Degree and 8+ years; OR Bachelor's Degree and 6+ years of clinical, technical, field service, medical device, healthcare, procedural support, or related experience.
Experience supporting device-based clinical, technical, procedural, or customer-facing activities, including physician education, device programming, troubleshooting, procedural support, or patient support.
Ability to work effectively in clinical environments while supporting multiple stakeholders and study priorities.
Ability to travel approximately 70% to 75% of the time, including overnight travel by air and automobile, to support clinical research sites and business needs across the United States.
Preferred Qualifications
Experience supporting clinical research studies, investigational device studies, feasibility studies, pivotal trials, or post-market clinical programs.
Experience with Neuromodulation and/or Pelvic Health therapies, including Deep Brain Stimulation, Spinal Cord Stimulation, Targeted Drug Delivery, Sacral Neuromodulation, Tibial Neuromodulation, or related therapy areas.
Experience providing procedural, operating room, interventional, or implant support, including device programming, follow-up care, and physician workflow support.
Knowledge of Good Clinical Practice, clinical trial conduct, protocol compliance, study documentation requirements, data quality standards, and regulated medical device environments.
Experience training, mentoring, coaching, or providing technical leadership to clinical, technical, or field-based professionals.
For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. 214.2(h)(4)(iii)(A) is required.
Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.
U.S. Work Authorization & Sponsorship
At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.
Recruitment Fraud Alert
We are aware of phishing scams targeting job seekers. Please keep the following in mind:
Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses.
Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate.
If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments.
If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at AskHR@medtronic.com.
Benefits & CompensationMedtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance,Health Savings Account,Healthcare Flexible Spending Account,Life insurance, Long-term disability leave,Dependent daycare spending account,Tuition assistance/reimbursement, andSimple Steps (global well-being program).
The following benefits and additional compensation are available to all regular employees:Incentive plans, 401(k) plan plus employer contribution and match,Short-term disability,Paid time off,Paid holidays,Employee Stock Purchase Plan,Employee Assistance Program,Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), andCapital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).
Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.
Further details are available at the link below:
Medtronic benefits and compensation plans
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can findhere a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
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