ZipRecruiter

Log In

1

Clinical Research Coordinator Trainee Jobs in Riverside, CA

Medix

Clinical Research Coordinator

Murrieta, CA · On-site

$31 - $38/hr

Must have oncology clinical research experience * Minimum of two years of clinical research experience Preferred Skills * Bachelor's degree preferred, but not required * Clinical skills highly ...

next page

Showing results 1-20

All JobsClinical Research JobsClinical Research Coordinator Trainee JobsClinical Research Coordinator Trainee Jobs in Riverside, CA

Clinical Research Coordinator Trainee information

See Riverside, CA salary details

$16

$29

$43

How much do clinical research coordinator trainee jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for clinical research coordinator trainee in Riverside, CA is $29.93, according to ZipRecruiter salary data. Most workers in this role earn between $24.33 and $32.36 per hour, depending on experience, location, and employer.

What is a clinical research coordinator trainee?

A Clinical Research Coordinator Trainee is an entry-level professional who assists with the daily operations of clinical research studies. They typically work under the supervision of experienced clinical research coordinators to learn how to manage clinical trials, ensure compliance with regulatory requirements, and maintain accurate study documentation. Trainees may help with participant recruitment, data collection, and communication between research teams and participants. This role provides foundational experience for a future career in clinical research management.

What are the key skills and qualifications needed to thrive as a clinical research coordinator trainee?

To thrive as a Clinical Research Coordinator Trainee, you need a background in life sciences or healthcare, understanding of clinical trial processes, and strong organizational skills, often supported by a bachelor's degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and regulatory documentation is typically required. Attention to detail, effective communication, and teamwork set standout candidates apart in this role. These skills ensure accurate study execution, regulatory compliance, and effective collaboration with research teams and study participants.

What are some typical challenges faced by clinical research coordinator trainees when managing multiple studies at once?

Clinical Research Coordinator Trainees often juggle several studies simultaneously, which can present challenges in time management, prioritizing tasks, and maintaining meticulous documentation for each trial. Balancing strict regulatory requirements with the day-to-day coordination of participant visits and data entry demands strong organizational skills and attention to detail. Trainees may also find it challenging to quickly adapt to different study protocols and collaborate effectively with investigators, sponsors, and other team members, but support from experienced coordinators and structured training can help overcome these hurdles.

What is the difference between Clinical Research Coordinator Trainee vs Clinical Research Coordinator?

AspectClinical Research Coordinator TraineeClinical Research Coordinator
CredentialsTypically pursuing or holds a relevant degree; may have some certificationUsually has completed training; often holds certifications like CCRP or CCRC
Work EnvironmentTraining setting, often supervised, in research facilities or hospitalsFull responsibilities in research sites, managing studies independently
Employer & Industry UsageEntry-level or training roles within research institutions or pharmaceutical companiesEstablished roles in clinical research teams across healthcare and pharma

The Clinical Research Coordinator Trainee is an entry-level position focused on learning and gaining experience under supervision, while the Clinical Research Coordinator is a fully responsible role managing clinical studies independently. The trainee is in a learning phase, whereas the coordinator has completed training and certification, handling day-to-day research activities.

Can you move up as a clinical research coordinator trainee?

A clinical research coordinator trainee can advance to a full clinical research coordinator role by gaining experience, demonstrating competence, and often obtaining relevant certifications such as CCRP. Career progression typically involves increasing responsibilities, specialized training, and sometimes further education in clinical research or related fields.

How to start as a clinical research coordinator?

To start as a clinical research coordinator, obtain a relevant bachelor's degree such as in health sciences, nursing, or biology. Gaining experience through internships or entry-level healthcare roles and obtaining certifications like the Certified Clinical Research Coordinator (CCRC) can improve job prospects. Strong organizational skills and familiarity with clinical trial protocols are also important for success in this role.

Is a clinical research coordinator an entry level job?

A clinical research coordinator trainee position is often considered entry level, suitable for individuals with a bachelor's degree in a related field. It typically involves on-the-job training and developing skills in study management, data collection, and regulatory compliance. Prior experience or certifications like Good Clinical Practice (GCP) can enhance job prospects but are not always required for entry-level roles.

What job categories do people searching Clinical Research Coordinator Trainee jobs in Riverside, CA look for?

The top searched job categories for Clinical Research Coordinator Trainee jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Clinical Research Coordinator Trainee jobs?

Cities near Riverside, CA with the most Clinical Research Coordinator Trainee job openings:

Clinical Research Coordinator Trainee jobs near you
Infographic showing various Clinical Research Coordinator Trainee job openings in Riverside, CA as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $62,248 per year, or $29.9 per hour.

Senior Clinical Research Coordinator

Headlands Research

Riverside, CA

$76K - $90K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 3 days ago

Job description

Artemis Research is a leading principal investigator- and patient-focused clinical research company dedicated to advancing medical treatments. Established in 2008 by colleagues who bring more than 50 years of combined research experience, Artemis specializes in Psychiatry/Neurology, Internal Medicine, and Women's Health studies. With multiple locations serving Southern California, including San Diego and Riverside, each Artemis site is fully equipped to conduct complex clinical research trials. 

Want to be a part of a growing company that's making a difference in our world? Look no further than Artemis Institute for Clinical Research! You'll enjoy a friendly and exciting culture with opportunities for growth and advancement. We offer the following generous benefits to our full-time employees:

  • A range of PPO and HMO medical plans
  • PPO and HMO dental plans
  • Vision coverage, long term disability plan, and life/AD&D coverage
  • 401k plan
  • Paid holidays and paid time off
  • A welcoming work environment

The Role

We are seeking an experienced Clinical Research Coordinator/Clinical Research Coordinator III for our Artemis Institute of Research clinical trial site located in Riverside, California. Under the supervision of the Site Director, the Senior Clinical Research Coordinator is responsible for the conduct of research protocols, such that the integrity and quality of the clinical research is maintained and the research is conducted in accordance with Good Clinical Practice Guidelines. 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: Monday through Friday, 9:30am-6:00pm

Responsibilities:

  • In-depth understanding of Pharmaceutical Sponsor/Industry initiated FDA studies in order to conduct the study with excellent quality
  • Managing all aspects of a study including participating in the informed consent process, coordinating and performing all visit study procedures per the protocol, entering data and query resolution, Investigational Product management, and managing all study related supplies and equipment, hosting monitoring visits, and attending investigator meetings
  • Experience managing multiple studies as the primary coordinator and someone ready to take the next step in managing people
  • Providing the highest level of care for study patients and delivering excellent customer service to the pharmaceutical clients

Qualifications:

  • Nursing license, medical assistant certificate or registration preferred
  • Minimum of two years of experience as a designated Clinical Research Coordinator on clinical trials required; sponsor-initiated and pharma clinical trials preferred
  • Previous clinical experience in a hands-on patient-facing role required
  • Commitment and ability to deliver excellent customer service
  • Excellent communication, punctual and responsible
  • Extremely well organized
  • Excellent verbal and written communication skills
  • Trustworthy, reliable; attentive to details
  • Mature and pleasant demeanor
  • Willingness to learn new tasks and grow with the company

Apply