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Cra Monitor Jobs (NOW HIRING)

IQVIA

CRA 2/Senior CRA

Dallas, TX

$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 ...

IQVIA

CRA 2/Senior CRA

Scottsdale, AZ

$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 ...

IQVIA

CRA 2/Senior CRA

Indianapolis, IN

$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 ...

IQVIA

CRA 2/Senior CRA

San Francisco, CA

$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 ...

IQVIA

CRA 2/Senior CRA

San Francisco, CA

$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 ...

IQVIA

CRA 2/Senior CRA

Scottsdale, AZ

$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 ...

IQVIA

CRA 2/Senior CRA

Durham, NC

$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 ...

IQVIA, Inc.

CRA 2/Senior CRA

Durham, NC · 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 ...

IQVIA

CRA 1, IQVIA Biotech

Ithaca, NY

$71K - $145K/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

Houston, TX

$71K - $145K/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

Boston, MA · On-site

$71K - $145K/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

Ithaca, NY

$71K - $145K/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

Bloomington, IL · On-site

$71K - $145K/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

San Francisco, CA

$71K - $145K/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 ...

Alira Health

Reviews monitoring visit reports, conducts co-monitoring and evaluation visits as needed. * Ensures ... Performs CRA mentoring. * Collaborates with development and maintenance of Clinical Trial ...

Cathay Bank

CRA Administration Officer (NE)

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

Kansas City, MO · On-site

$71K - $145K/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

San Antonio, TX

$71K - $145K/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

$71K - $145K/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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Showing results 41-60

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 Aug 12, 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.

Is a CRA monitor an entry level job?

A CRA monitor role is typically considered an entry-level or early-career position in clinical research, often requiring a bachelor's degree in a related field and some experience with monitoring or clinical trials. It involves overseeing trial sites, ensuring compliance, and may require familiarity with regulatory guidelines and monitoring tools. Advancement usually depends on experience and additional certifications such as RAC or CCRA.

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.

What are the key skills and qualifications needed to thrive as a CRA monitor?

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 is a CRA monitor?

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 are some common challenges 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.

Is it hard to get a CRA Monitor job?

Getting a CRA Monitor position can be competitive and typically requires relevant experience in clinical research, knowledge of regulatory guidelines, and often a bachelor's degree in a related field. Strong organizational skills and familiarity with monitoring tools can improve chances, but the hiring process varies by employer and location.
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 August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 13% Part Time, 1% Temporary, 4% Contract, and 1% Nights. 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.

CRA 2/Senior CRA

IQVIA

Dallas, TX

$90K - $175K/yr

Full-time

Re-posted 11 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

60th of 223 rated it services

Job description

IQVIA Biotech is seeking CRA 2 and Sr. CRA 1 candidates with onsite monitoring experience in oncology.

Join a Team That's Advancing Clinical Research

We're looking for a passionate and driven Clinical Research Associate (CRA) to join our 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

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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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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