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Cra Ii Jobs (NOW HIRING)

410 ICR United States USA

CRA 2

Blue Bell, PA

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do: You ...

410 ICR United States USA

CRA 2

Blue Bell, PA

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do: You ...

Icon plc

CRA 2

Blue Bell, PA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do: You ...

410 ICR United States USA

CRA 2

Blue Bell, PA

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do: You ...

ICON

Clinical Research Associate

Blue Bell, PA · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do: You ...

Icon plc

CRA 2

Blue Bell, PA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do: You ...

ICON

CRA 2

Blue Bell, PA · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do: You ...

ICON

CRA 2

Blue Bell, PA · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do: You ...

ICON

CRA 2

Blue Bell, PA · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do: You ...

IQVIA

CRA 2/Senior CRA

Phoenix, AZ · On-site

$90K - $175K/yr

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 ...

ICON

CRA 2

Blue Bell, PA · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do: You ...

IQVIA

CRA 2/Senior CRA

New York, NY

$90K - $175K/yr

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 ...

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 oncology. Join a Team That's Advancing Clinical Research We're looking for a passionate and driven ...

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 oncology. Join a Team That's Advancing Clinical Research We're looking for a passionate and driven ...

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 oncology. Join a Team That's Advancing Clinical Research We're looking for a passionate and driven ...

IQVIA

CRA 2/Senior CRA

Sacramento, CA · On-site

$90K - $175K/yr

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 ...

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 oncology. Join a Team That's Advancing Clinical Research We're looking for a passionate and driven ...

Icon plc

CRA 2

Blue Bell, PA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do: You ...

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 oncology. Join a Team That's Advancing Clinical Research We're looking for a passionate and driven ...

IQVIA

CRA 2/Senior CRA

Sacramento, CA · On-site

$90K - $175K/yr

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 ...

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Showing results 21-40

All JobsCra Ii Jobs

Cra Ii information

See salary details

$12

$41

$69

How much do cra ii jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for cra ii 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 II (CRA II), and why are they important?

To thrive as a CRA II, you need a solid background in clinical research, knowledge of Good Clinical Practice (GCP), and typically a bachelor's degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, regulatory documentation, and clinical trial management software is essential. Strong attention to detail, organizational skills, and effective communication help build trust with study sites and ensure protocol adherence. These competencies are crucial for maintaining data integrity, regulatory compliance, and the overall success of clinical trials.

What are some common challenges CRA IIs face when managing multiple clinical trial sites simultaneously?

As a CRA II, juggling several clinical trial sites can present challenges such as coordinating site visits, maintaining timely communication, and ensuring protocol compliance across diverse teams. Effective time management, organization, and proactive problem-solving are essential to address site-specific issues and keep studies on track. Additionally, balancing travel demands with documentation and reporting requirements can be demanding, so strong prioritization and adaptability are key for success in this role.

What is the difference between Cra Ii vs Cra I?

AspectCra ICra II
Required CertificationsTypically requires a basic certification or no certificationRequires advanced certification or more experience
Work EnvironmentEntry-level clinical research settingsMore complex projects, increased responsibilities
Job ResponsibilitiesAssisting with data collection and basic tasksOverseeing data, coordinating activities, mentoring Cra I
Industry UsageCommonly used in clinical research organizations and pharmaUsed in similar settings but with higher responsibility

The main difference between Cra I and Cra II lies in experience, responsibilities, and certifications. Cra II roles involve more complex tasks, greater oversight, and often require additional certifications, reflecting a higher level of expertise in clinical research.

What is a CRA II?

CRA II stands for Clinical Research Associate II. These professionals are responsible for monitoring clinical trials to ensure compliance with regulatory requirements and study protocols. They serve as a key link between the clinical trial site and the sponsor or CRO, overseeing data integrity, patient safety, and proper documentation. CRA IIs typically have more experience than entry-level CRAs and may handle more complex trials or sites.
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Cra Ii jobs near you
Infographic showing various Cra Ii job openings in the United States as of August 2026, with employment types broken down into 92% Full Time, 5% Part Time, 1% Temporary, and 2% Contract. Highlights an 81% Physical, 6% Hybrid, and 13% Remote job distribution, with an average salary of $85,542 per year, or $41.1 per hour.

CRA 2

410 ICR United States USA

Blue Bell, PA

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 8 days ago

Job description

Clinical Research Associate

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 CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What You Will Do:

You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:

  • 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:

You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.
Required qualifications and experience:

  • Bachelor's degree in a scientific or healthcare-related field.
  • Minimum of 2 years of experience as a 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.
  • 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