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Cra Monitoring Jobs (NOW HIRING)

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CRA II and Senior CRA

Houston, TX · Remote

$91K - $114K/yr

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

IQVIA

CRA 2/Senior CRA

New York, NY · 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 2/Senior CRA

Sacramento, 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

Dallas, TX · 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 2/Senior CRA

Houston, TX · 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 2/Senior CRA

Chicago, IL

$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

Carlsbad, 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

Phoenix, 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 · 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 2/Senior CRA

Houston, 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

Gilbert, 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

Phoenix, 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

Carlsbad, 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 ...

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Showing results 21-40

All JobsCra Monitoring Jobs

CRA Monitoring information

See salary details

$12

$41

$69

How much do cra monitoring jobs pay per hour?

As of Aug 11, 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.

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.
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:
CRA Monitoring jobs near you
Infographic showing various Cra Monitoring job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 10% Part Time, and 5% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $85,542 per year, or $41.1 per hour.

CRA II and Senior CRA

Icon plc

Houston, TX • Remote

$91K - $114K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 29 days ago

Job description

CRA II or Senior CRA (Home-based in U.S.)

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


We are currently seeking a Clinical Research Associate (Level II or Senior) to join our diverse and dynamic team. As a CRA II/Senior CRA at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing

  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.

  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.

  • Collaborating with investigators and site staff to facilitate smooth study conduct.

  • Performing data review and resolution of queries to maintain high-quality clinical data.

  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports


Your profile

  • Bachelor's degree in a scientific or health-related field or an equivalent combination of education and clinical research experience, particularly in a study coordinator or nursing role.

  • Minimum of 1 year independent monitoring to be considered for a Clinical Research Associate II and a minimum of 3 years independent monitoring to be considered for a Senior Clinical Research Associate.

  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.

  • Strong organizational and communication skills, with attention to detail.

  • Ability to work independently and collaboratively in a fast-paced environment.

  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver's license

#LI-MM2

#LI-Remote


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.

Salary Range

$91,336.00-$114,170.00

Are you a current ICON Employee? Please click here to apply

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