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Cra Monitoring Jobs (NOW HIRING)

You'll own RDI's clinical-monitoring standard, level up the team by reviewing their real work alongside them, and serve as the senior point of judgment for the hardest monitoring questions. It's a ...

New

Clinical Research Monitor (CRA) Location: Remote Position overview: * We are hiring an experienced Clinical Research Associate (CRA) to support and monitor clinical trials across multiple sites.

CRA- Analyst

Minneapolis, MN ยท On-site

$30 - $32/hr

Evaluate, monitor, and document study results. * Exercise good clinical judgment and demonstrate ... In-house pharma CRA experience (strictly Regional CRA experience will be considered) * Clinical ...

Evaluate, monitor, and document study results. * Exercise good clinical judgment and demonstrate ... In-house pharma CRA experience (strictly Regional CRA experience will be considered) * Clinical ...

Oversight and monitoring of CRA service hour volumes and reporting accuracy. * Promoting and coordinating bank-wide volunteer opportunities through events module. * Partnering with internal teams and ...

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

Oversight and monitoring of CRA service hour volumes and reporting accuracy. * Promoting and coordinating bank-wide volunteer opportunities through events module. * Partnering with internal teams and ...

Oversight and monitoring of CRA service hour volumes and reporting accuracy. * Promoting and coordinating bank-wide volunteer opportunities through events module. * Partnering with internal teams and ...

Oversight and monitoring of CRA service hour volumes and reporting accuracy. * Promoting and coordinating bank-wide volunteer opportunities through events module. * Partnering with internal teams and ...

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

CRA 2/Senior CRA

Dallas, TX ยท On-site

$90K - $175K/yr

IQVIA Biotech is seeking CRA 2 and Sr. CRA 1 candidates with onsite monitoring experience in ... Lead and execute site monitoring visits (selection, initiation, routine, and close-out) in ...

CRA 2/Senior CRA

Sacramento, CA ยท On-site

$90K - $175K/yr

IQVIA Biotech is seeking CRA 2 and Sr. CRA 1 candidates with onsite monitoring experience in ... Lead and execute site monitoring visits (selection, initiation, routine, and close-out) in ...

CRA 2/Senior CRA

Phoenix, AZ ยท On-site

$90K - $175K/yr

IQVIA Biotech is seeking CRA 2 and Sr. CRA 1 candidates with onsite monitoring experience in ... Lead and execute site monitoring visits (selection, initiation, routine, and close-out) in ...

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

CRA 2/Senior CRA

New York, NY ยท On-site

$90K - $175K/yr

IQVIA Biotech is seeking CRA 2 and Sr. CRA 1 candidates with onsite monitoring experience in ... Lead and execute site monitoring visits (selection, initiation, routine, and close-out) in ...

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Cra Monitoring information

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$12

$41

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How much do cra monitoring jobs pay per hour?

As of Jun 5, 2026, the average hourly pay for cra monitoring in the United States is $41.13, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $52.64 per hour, depending on experience, location, and employer.

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

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 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.

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 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.

More about Cra Monitoring jobs
What states have the most Cra Monitoring jobs? States with the most job openings for Cra Monitoring jobs include:
What job categories do people searching Cra Monitoring jobs look for? The top searched job categories for Cra Monitoring jobs are:
Infographic showing various Cra Monitoring job openings in the United States as of May 2026, with employment types broken down into 90% Full Time, and 10% Part Time. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $85,542 per year, or $41.1 per hour.

Global CRA - Monitoring & Compliance

Alira Health Boston, LLC

Manhattan, NY โ€ข On-site

Full-time

Posted 4 days ago


Job description

Alira Health Boston, LLC is seeking a dedicated Site Monitor to ensure compliance and the quality of clinical trials. This role involves performing site monitoring visits, providing training, and collaborating across teams to maintain high standards of clinical trial conduct. The ideal candidate should have a Bachelor's degree in a relevant field and experience in the pharmaceutical or healthcare industry.

The position offers a competitive salary and the opportunity to contribute to innovative healthcare solutions. #J-18808-Ljbffr