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Cra Monitor Jobs (NOW HIRING)

Contract CRA

Covington, KY ยท On-site

$90 - $100/hr

The ideal candidate will have a strong background in site monitoring and clinical trial management ... This is a home-based position for a CRA located in the Midwest/ Central U.S. region, with regular ...

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 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

San Francisco, 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 ...

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 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

Durham, NC 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 ...

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

Durham, NC 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 ...

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

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 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 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 ...

CRA 1, IQVIA Biotech

Kansas City, MO ยท 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 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 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 ...

CRA Administration Officer (NE)

El Monte, CA ยท 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 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 ...

CRA 1, IQVIA Biotech

Fort Worth, TX ยท 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 1-20

Cra Monitor information

See salary details

$11K

$79.4K

$137.5K

How much do cra monitor jobs pay per year?

As of Jul 21, 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 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.

Is it hard to get a CRA job?

Securing a CRA (Clinical Research Associate) position can be competitive, often requiring relevant education such as a degree in life sciences or healthcare, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and certifications like ACRP or SOCRA can improve job prospects, but entry may be challenging for those without related experience or credentials.

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 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 salary for CRA?

The salary for a CRA (Clinical Research Associate) typically ranges from $55,000 to $95,000 annually, depending on experience, location, and the employer. Entry-level CRAs may start around $50,000, while experienced professionals with specialized skills can earn over $100,000. Certifications like CCRP can also influence salary levels.

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.

How to become a clinical trial monitor?

To become a clinical trial monitor, typically one needs a bachelor's degree in health sciences, nursing, or a related field, along with experience in clinical research. Certification such as the Certified Clinical Research Professional (CCRP) can enhance job prospects, and familiarity with Good Clinical Practice (GCP) guidelines and clinical trial management systems is often required.

What is a CRA monitor?

A CRA monitor is a professional responsible for overseeing clinical trial sites to ensure compliance with regulatory requirements and study protocols. They typically conduct site visits, review documentation, and verify data accuracy, often requiring knowledge of Good Clinical Practice (GCP) and relevant regulations. The role involves travel and collaboration with research teams to ensure trial integrity.
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:
Infographic showing various Cra Monitor job openings in the United States as of July 2026, with employment types broken down into 3% Locum Tenens, 87% Full Time, 3% Part Time, 1% Contract, and 6% Summer. Highlights an 83% Physical, 4% Hybrid, and 13% Remote job distribution, with an average salary of $79,437 per year, or $38.2 per hour.
Contract CRA

Contract CRA

Solomon Page

Covington, KY โ€ข On-site

$90 - $100/hr

Contractor

Medical, Dental, Retirement

Posted 28 days ago


Job description

We are seeking an experienced and highly motivated Clinical Research Associate (CRA) to support a Phase 2 clinical trial in the lung transplant therapeutic area. The ideal candidate will have a strong background in site monitoring and clinical trial management, with direct experience supporting pulmonary or transplant studies. This is a home-based position for a CRA located in the Midwest/ Central U.S. region, with regular travel to assigned investigative sites across the United States.
  • Location: Midwest/Central United States (Home-Based)
  • Employment Type: 1.0 FTE Contract
  • Contract Duration: 6 Months with Possibility of Extension
  • Start Date: ASAP
  • Therapeutic Area: Lung Transplant
  • Clinical Trial Phase: Phase IIPay Rate: $90-100/hr

?
Required Qualifications:
  • Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
  • Minimum 5 years of Clinical Research Associate (CRA) experience.
  • Direct monitoring experience in pulmonary transplant and/or lung transplant clinical studies is required.
  • Strong understanding of ICH-GCP, FDA regulations, and clinical trial processes.
  • Experience managing high-performing academic medical center sites.
  • Excellent organizational, communication, and problem-solving skills.
  • Ability to travel regularly to assigned study sites.

If you meet the required qualifications and are interested in this role, please apply today.
The Solomon Page Distinction
Solomon Page offers a comprehensive benefit program for hourly employees. We pride ourselves on offering medical, dental, 401(k), direct deposit and commuter benefits to our employees, including freelancers - which sets us apart in the industries we serve.
About Solomon Page
Founded in 1990, Solomon Page is a specialty niche provider of staffing and executive search solutions across a wide array of functions and industries. The success of Solomon Page reflects an organic growth strategy supported by a highly entrepreneurial culture. Acting as a strategic partner to our clients and candidates, we focus on providing customized solutions and building long-term relationships based on trust, respect, and the consistent delivery of excellent results. For more information and additional opportunities, visit: solomonpage.com and connect with us on Facebook , and LinkedIn .
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