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Cra Monitoring Jobs in California (NOW HIRING)

krg technology inc

CRA Wiz App Consultant

Pasadena, CA · On-site

CRA Wiz App Consultant Location: Pasadena, Ca Duration: Contract / Full Time Utilize CRA Wiz : The ... The solution includes more than a hundred pre-programmed reports to help you analyze, monitor and ...

Mindlance

Clinical Research Assocoate

San Diego, CA · On-site

... CRA Certification Responsibilities Support assigned study teams with TMF set-up, maintenance, ongoing quality control reviews, and final reconciliation of study documents * Routinely monitor TMF ...

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Senior CRA

Los Angeles, CA · On-site

$110K - $138K/yr

Senior CRA Phase I Oncology- CA ICON is a global healthcare intelligence and clinical research ... Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ...

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Senior CRA

Mcfarland, CA

Senior CRA- Phase I Oncology/Mountain West-IA/UT/CO/KS/NE ICON is a global healthcare intelligence ... Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ...

410 ICR United States USA

Senior CRA

Los Angeles, CA · On-site

$110K - $138K/yr

Senior CRA Phase I Oncology- CA ICON is a global healthcare intelligence and clinical research ... Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ...

Icon plc

Senior CRA

Long Beach, CA · On-site

$110K - $138K/yr

Senior CRA Phase I Oncology- CA ICON is a global healthcare intelligence and clinical research ... Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ...

410 ICR United States USA

Senior CRA

Long Beach, CA

$110K - $138K/yr

Senior CRA Phase I Oncology- CA ICON is a global healthcare intelligence and clinical research ... Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ...

Ardelyx

In House Clinical Research Associate

Newark, CA · On-site +1

$99K - $121K/yr

The Clinical Research Associate (CRA) supports sponsor oversight of clinical trial execution with ... Monitor site performance through centralized and remote review of study data, key performance ...

5PY IQVIA RDS Inc.

$47K - $169K/yr

Req • Equivalent combination of education, training and experience may be accepted in lieu of degree. • Some organizations require completion of CRA training program or prior monitoring ...

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All JobsCra Monitoring JobsCra Monitoring Jobs in California

Cra Monitoring information

See California salary details

$11

$40

$68

How much do cra monitoring jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for cra monitoring in California is $40.59, according to ZipRecruiter salary data. Most workers in this role earn between $28.46 and $51.97 per hour, depending on experience, location, and employer.

How hard is it to get a CRA Monitoring job?

Securing a CRA Monitoring position typically requires relevant experience in clinical research, knowledge of Good Clinical Practice (GCP), and often a bachelor's degree in a health-related field. Many employers prefer candidates with previous monitoring or clinical trial management experience, and certifications like CCRP can improve job prospects. The hiring process can be competitive, depending on the level of experience and specific requirements of the role.

What are some common challenges faced by CRA monitoring professionals when conducting site visits, and how can they be addressed?

CRA Monitoring professionals often encounter challenges such as inconsistent site documentation, varying levels of site staff experience, and ensuring compliance with complex regulatory requirements. To address these, effective communication with site staff, thorough preparation before each visit, and continuous training on protocol and regulatory updates are essential. Building strong relationships with clinical sites and proactively identifying potential issues can also help ensure successful monitoring and trial progress.

Is CRA monitoring an entry level job?

CRA monitoring roles are often considered entry-level positions in clinical research, suitable for individuals with a basic understanding of Good Clinical Practice (GCP) and regulatory requirements. These roles typically require strong attention to detail, organizational skills, and sometimes a relevant degree or certification, but they generally do not require extensive prior experience.

What qualifications do I need to be a CRA?

A Clinical Research Associate (CRA) typically needs a bachelor's degree in life sciences, healthcare, or a related field. Relevant experience in clinical trials, knowledge of Good Clinical Practice (GCP) guidelines, and strong organizational skills are also important; some roles may require certification such as the RAC or CCRP.

What is the difference between Cra Monitoring vs Clinical Research Associate Monitoring?

AspectCra MonitoringClinical Research Associate Monitoring
CredentialsTypically requires a degree in life sciences or healthcare, with certifications like CCRP or RACRequires similar degrees and certifications, often CCRP or RAC
Work EnvironmentWorks primarily on clinical trial sites and in officesWorks on-site at clinical trial locations and in monitoring offices
Industry UsageCommonly used term in clinical trial monitoring rolesOften used interchangeably with Cra Monitoring in job listings
Job ResponsibilitiesMonitoring trial progress, ensuring compliance, data verificationMonitoring trial progress, site management, regulatory compliance

Cra Monitoring and Clinical Research Associate Monitoring are often used interchangeably, both involving site visits, data verification, and ensuring compliance in clinical trials. The main difference lies in terminology preference, but the roles and requirements are very similar, making them essentially the same job in different words.

What is CRA monitoring?

CRA monitoring refers to the process in which a Clinical Research Associate (CRA) oversees clinical trials to ensure they are conducted according to the study protocol, Good Clinical Practice (GCP), and regulatory requirements. The CRA visits clinical trial sites to verify data accuracy, monitor patient safety, and ensure proper documentation. Monitoring helps maintain the integrity of the research and ensures reliable data collection for the study. CRAs play a vital role in identifying and resolving issues that may arise during the trial. Their work helps uphold ethical standards and regulatory compliance in clinical research.

What are the key skills and qualifications needed to thrive as a clinical research associate in monitoring?

To thrive as a CRA in Monitoring, you need a solid background in life sciences, familiarity with clinical trial processes, and often a relevant degree or certification such as ACRP or SOCRA. Proficiency in electronic data capture (EDC) systems, trial management software, and regulatory compliance tools is typically required. Exceptional attention to detail, strong organizational skills, and effective communication are soft skills that set top performers apart. These competencies are crucial for ensuring data integrity, regulatory adherence, and smooth collaboration between clinical sites and sponsors.
What are popular job titles related to Cra Monitoring jobs in California? For Cra Monitoring jobs in California, the most frequently searched job titles are:
What job categories do people searching Cra Monitoring jobs in California look for? The top searched job categories for Cra Monitoring jobs in California are:
Cra Monitoring jobs near you
Infographic showing various Cra Monitoring job openings in California as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 11% Part Time, 2% Temporary, and 4% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $84,422 per year, or $40.6 per hour.

CRA 2/Senior CRA - FSP Sponsor Dedicated

IQVIA

Carlsbad, CA • On-site

$90K - $175K/yr

Full-time

Posted 12 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

61st of 223 rated it services

Job description

Join a Team That's Advancing Clinical Research

Travel: Regional 65-70%

We're looking for a passionate and driven Clinical Research Associate (CRA) 1-3 years of on-site monitoring experience to join our FSP Sponsor Dedicated team and play a key role in delivering high-quality clinical trials. In this role, you'll partner with investigative sites and cross-functional teams to ensure studies are executed with excellence, compliance, and patient focus.

What You'll Do
  • Lead and execute site monitoring visits (selection, initiation, routine, and close-out) in accordance with GCP/ICH guidelines
  • Build strong relationships with investigative sites to drive performance, recruitment, and engagement
  • Ensure protocol compliance, data integrity, and high-quality study execution
  • Proactively identify risks, resolve issues, and escalate when needed
  • Track and manage study progress, including regulatory approvals, enrollment, and data quality
  • Maintain accurate documentation and contribute to inspection readiness
  • Collaborate with cross-functional teams to ensure successful study delivery
What You Bring
  • Bachelor's degree in life sciences, healthcare, or related field (or equivalent experience)
  • 1+ year of on-site monitoring experience
  • Solid understanding of GCP, ICH, and regulatory requirements
  • Strong communication, problem-solving, and organizational skills
  • Ability to manage multiple priorities in a fast-paced environment

Why Join Us

Make a direct impact on advancing clinical research and improving patient outcomes

  • Work alongside experienced, collaborative teams
  • Opportunities for growth and career development
  • Dynamic, fast-paced environment where your contributions matter

If you're ready to take the next step in your CRA career and be part of meaningful, impactful work, we'd love to hear from you.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $90,200.00 - $175,100.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

What IQVIA employees say

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Benefits

Hours and flexibility

Workplace

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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