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Cra Monitoring Jobs in New York (NOW HIRING)

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Senior CRA

Basking Ridge, NJ · On-site

Senior CRA ICON is a global healthcare intelligence and clinical research organisation united by a ... Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ...

ICON

Senior CRA

Farmingdale, NY · On-site +1

$110K - $138K/yr

Senior CRA Phase I Oncology- NY/NJ ICON is a global healthcare intelligence and clinical research ... Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ...

Icon plc

Senior CRA

Farmingdale, NY

$110K - $138K/yr

Senior CRA Phase I Oncology- NY/NJ ICON is a global healthcare intelligence and clinical research ... Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ...

Icon plc

Senior CRA

New York, NY · On-site

$110K - $138K/yr

Senior CRA- Phase I Oncology/NJ/NY ICON is a global healthcare intelligence and clinical research ... Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ...

410 ICR United States USA

Senior CRA

Farmingdale, NY

$110K - $138K/yr

Senior CRA Phase I Oncology- NY/NJ ICON is a global healthcare intelligence and clinical research ... Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ...

410 ICR United States USA

Senior CRA

Farmingdale, NY · On-site

$110K - $138K/yr

Senior CRA Phase I Oncology- NY/NJ ICON is a global healthcare intelligence and clinical research ... Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ...

ICON

Senior CRA

New York, NY · On-site +1

$110K - $138K/yr

Senior CRA - Onc - NorthEast ICON is a global healthcare intelligence and clinical research ... Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ...

Icon plc

Senior CRA

New York, NY · On-site

$110K - $138K/yr

Senior CRA Phase I Oncology- NY/NJ ICON is a global healthcare intelligence and clinical research ... Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ...

Icon plc

Senior CRA

New York, NY · On-site

$110K - $138K/yr

Senior CRA- Phase I Oncology/NY/NJ ICON is a global healthcare intelligence and clinical research ... Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ...

IQVIA

Clinical Research Associate

Parsippany, NJ

$71K - $189K/yr

Clinical Research Associate II & Senior Clinical Research Associate (CRA II/Sr. CRA) Multiple ... Conduct all phases of site monitoring activities, including site selection, initiation, routine ...

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Showing results 21-40

All JobsCra Monitoring JobsCra Monitoring Jobs in New York

Cra Monitoring information

See New York salary details

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$44

$76

How much do cra monitoring jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for cra monitoring in New York is $44.99, according to ZipRecruiter salary data. Most workers in this role earn between $31.54 and $57.60 per hour, depending on experience, location, and employer.

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.

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 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.

How hard is it to get a CRA Monitoring job?

A CRA Monitoring job typically requires relevant experience in clinical research, knowledge of Good Clinical Practice (GCP), and often a bachelor's degree in a health-related field. Competition can be moderate, and strong organizational skills, attention to detail, and familiarity with clinical trial management systems improve chances of hiring. Certifications like RAC or CCRP can also enhance prospects.

What are popular job titles related to Cra Monitoring jobs in New York?

For Cra Monitoring jobs in New York, the most frequently searched job titles are:

What job categories do people searching Cra Monitoring jobs in New York look for?

The top searched job categories for Cra Monitoring jobs in New York are:

Cra Monitoring jobs near you
Infographic showing various Cra Monitoring job openings in New York as of August 2026, with employment types broken down into 1% As Needed, 88% Full Time, 8% Part Time, and 3% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $93,586 per year, or $45 per hour.

Senior CRA

410 ICR United States USA

Basking Ridge, NJ

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 17 days ago

Job description

Senior CRA

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.


As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.

What You Will Do:

You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.
Key responsibilities include:

  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
  • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
  • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
  • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
  • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.
Required qualifications and experience:

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
  • Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
  • Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
  • Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
  • Willingness to travel as required (approximately 60%)

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 request here.

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