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Cra Monitor Jobs (NOW HIRING)

Eisenhower

Clinical Research Associate

Rancho Mirage, CA · On-site

$20.71 - $31.30/hr

... CRA/monitor/IRB.7. Reports serious adverse events.8. Handles and maintains investigator files.9. Schedules meetings with physicians, creates agendas, and takes minutes.10. Sends letters and/or ...

Cathay Bank

CRA Administration Officer

El Monte, CA · On-site

$33.65 - $48.08/hr

Monitor reports and prepare quarterly performance analysis, annual self-assessment, strategic plan ... CRA knowledge is a plus. Knowledge of CRA software and SharePoint preferred. * Skills/Ability:

IQVIA

CRA 1, IQVIA Biotech

Durham, NC

$71.90K - $119.90K/yr

IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring ... Must have experience monitoring in oncology solid tumor. IQVIA Biotech is a full-service CRO ...

ICON plc

CRA II and Senior CRA

Chicago, IL · Remote

CRA II/Senior CRA (Home-based anywhere in the U.S.) ICON plc is a world-leading healthcare ... Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.

IQVIA

CRA 1, IQVIA Biotech

Rockville, MD · On-site

$71.90K - $119.90K/yr

IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring ... Must have experience monitoring in oncology solid tumor. IQVIA Biotech is a full-service CRO ...

IQVIA

CRA 1, IQVIA Biotech

Las Vegas, NV · On-site

$71.90K - $119.90K/yr

IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring ... Must have experience monitoring in oncology solid tumor. IQVIA Biotech is a full-service CRO ...

IQVIA

CRA 1, IQVIA Biotech

Collegeville, PA · On-site

$71.90K - $119.90K/yr

IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring ... Must have experience monitoring in oncology solid tumor. IQVIA Biotech is a full-service CRO ...

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All JobsCra Monitor Jobs

Cra Monitor information

See salary details

$11K

$79.4K

$137.5K

How much do cra monitor jobs pay per year?

As of Jun 2, 2026, the average yearly pay for cra monitor in the United States is $79,437.00, according to ZipRecruiter salary data. Most workers in this role earn between $33,000.00 and $136,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a CRA (Clinical Research Associate) Monitor, and why are they important?

To thrive as a CRA Monitor, you need a solid understanding of clinical trial protocols, regulatory guidelines (such as GCP), and a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like ACRP or SOCRA are commonly required. Strong attention to detail, communication, and problem-solving skills help build trust with site staff and ensure trial integrity. These skills ensure accurate data collection, regulatory compliance, and the smooth progress of clinical trials.

What are some common challenges Clinical Research Associate (CRA) Monitors face when working across multiple study sites?

CRA Monitors often juggle several clinical trial sites simultaneously, which can present challenges such as coordinating schedules, ensuring consistent protocol adherence, and managing diverse site staff. They need to be adept at prioritizing tasks, maintaining detailed documentation, and swiftly resolving site-specific issues. Effective communication and strong organizational skills are crucial for building good relationships with site staff and ensuring that trials progress smoothly and compliantly.

What are CRA Monitors?

CRA Monitors, also known as Clinical Research Associates (CRAs), are professionals responsible for overseeing clinical trials to ensure they are conducted in accordance with regulatory requirements, study protocols, and ethical guidelines. They act as the main point of contact between the study sponsor and the research sites, monitoring patient safety, data accuracy, and compliance throughout the trial. Their duties include site visits, reviewing case report forms, and ensuring proper documentation, ultimately ensuring the integrity and quality of clinical research.

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

AspectCra MonitorClinical Research Associate
CertificationsTypically requires GCP training, CRA certification (e.g., SOCRA, ACRP)Same certifications as Cra Monitor, often with additional site management training
Work EnvironmentPrimarily monitors clinical trials remotely or on-site at sitesWorks on-site at clinical trial sites, overseeing patient recruitment and data collection
Employer & Industry UsageUsed by pharmaceutical companies, CROs, biotech firmsCommonly employed by CROs, pharmaceutical companies, and research institutions

The Cra Monitor and Clinical Research Associate roles are closely related, with both requiring similar certifications and working within the clinical trial industry. The main difference lies in their focus: Cra Monitors primarily oversee trial compliance and data integrity, often remotely, while Clinical Research Associates are more involved in site management and patient interactions on-site. Both roles are essential in ensuring the success of clinical studies.

More about Cra Monitor jobs
What are the most commonly searched types of Cra Monitor jobs? The most popular types of Cra Monitor jobs are:
What job categories do people searching Cra Monitor jobs look for? The top searched job categories for Cra Monitor jobs are:
Cra Monitor jobs near you
Infographic showing various Cra Monitor job openings in the United States as of May 2026, with employment types broken down into 7% Full Time, 11% Temporary, and 82% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $79,437 per year, or $38.2 per hour.

Clinical Research Associate

Eisenhower

Rancho Mirage, CA • On-site

$20.71 - $31.30/hr

Full-time

Posted 2 days ago

Job description

Default Work Shift:

Varies (United States of America)

Hours:

40

Salary range:

$20.71 - $31.30

Schedule:

Full Time

Shift Hours:

8 Hour employee

Department:

Research-Other

Job Objective:

Assists in the running of Clinical Trials.

Job Description:

Education:Required: Bachelor's degree or two (2) years' research experience in lieu of degree; completion of CITI Good Clinical Practice (GCP) for Clinical Trials with Investigational Drugs and Medical Devices (U.S. FDA Focus) course (www.CITIprogram.org)Preferred: Bachelor's degree in Clinical Research, Nursing or AdministrationLicensure/Certification:Required: Certification from Society of Clinical Research Associate (SOCRA) as a Certified Clinical Research Professional (CCRP) or Certification from Association of Clinical Research Professionals (ACRP), such as, Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Associate (CCRA), ACRP Certified Professional (ACRP-CP) within two (2) years (full-time employee) or four (4) years (part-time employee) of hireExperience:Required: One (1) year of healthcare experience or successful completion of paid six (6) month Research Internship at Eisenhower HealthReports To: Manager-Research and Clinical TrialsSupervises: N/AAges of Patients: Adult, GeriatricBlood Borne Pathogens: Moderate Potential

Skills, Knowledge, Abilities:

Ability to create a welcoming environment for patients and visitors, demonstrating empathy and respect in all interactions, Ability to organize information or data to facilitate easy retrieval and use, Ability to prioritize tasks and manage time efficiently to meet deadlines, Ability to use Microsoft Office Suite (Word, Excel, Outlook, PowerPoint) and other relevant software applications, Written and verbal communication skills

Essential Responsibilities

1. Demonstrates compliance with Code of Conduct and compliance policies, and takes action to resolve compliance questions or concerns and report suspected violations.2. Completes patient screening for eligibility to research protocol; records results in logs and Epic.3. Completes registration/randomization to protocol; schedules treatment, specimen collection, imaging studies and/or other tests/exams.4. Completes patient recruitment and follow-up.5. Completes case report forms (CRFs); ensures adequate source documentation in the medical record to support clinical trial; abstracts data from Epic (source data) and/or obtains medical records to complete CRFs; contacts patient, as needed, to collect data and documents in Epic; completes data entry in electronic data capture (EDC) or specified databases; resolves queries.6. Reports and communicates to the sponsor/CRA/monitor/IRB.7. Reports serious adverse events.8. Handles and maintains investigator files.9. Schedules meetings with physicians, creates agendas, and takes minutes.10. Sends letters and/or telephones/communicates with patients and physicians regarding study results.11. Performs other duties as assigned.

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