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Clinical Research Associate Ii Jobs (NOW HIRING)

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... Clinical Research Associates across North America ... As we expand our partnerships with leading global sponsors, we are seeking experienced CRA II and ...

Avania

Clinical Research Associate II

$90K - $110K/yr

Avania is hiring Clinical Research Associates II (CRA II) - Medical Device Clinical Trials Salary range $90,000 - $110,000 + Annual performance related bonus + Benefits - Minimum 2+ years of prior ...

New

Emmes

Clinical Research Associate II

Rockville, MD · On-site +1

Overview Clinical Research Associate II US remotely and on-site (80% travel) Be Part of One Team, One Purpose. At Emmes Group , we're shaping the future of clinical research- where human intelligence ...

ICON

Clinical Research Associate II

Blue Bell, PA · On-site

We are currently seeking a Senior Clinical Research Associate or Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal ...

ClinChoice

We're currently expanding our CRA network in the Netherlands and looking for talented Clinical Research Associates (CRA II and Senior CRA) interested in partnering with some of the world's leading ...

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Clinical Research Associate 2

Chicago, IL · On-site

$91K - $114K/yr

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 ...

ICON

Clinical Research Associate 2

Chicago, IL · On-site +1

$91K - $114K/yr

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 ...

IQVIA

Clinical Research Associate 2, IQVIA

Durham, NC · On-site

$71K - $189K/yr

IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in IM/GI, MASH/NASH, dermatology and/or asthma/respiratory clinical trials. Women's Health experience is a plus! Job ...

IQVIA

Clinical Research Associate 2, IQVIA

Durham, NC · On-site

$71K - $189K/yr

IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in IM/GI, MASH/NASH, dermatology and/or asthma/respiratory clinical trials. Women's Health experience is a plus! Job ...

IQVIA, Inc.

Clinical Research Associate 2, IQVIA

Durham, NC · On-site

$71K - $189K/yr

IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in IM/GI, MASH/NASH, dermatology and/or asthma/respiratory clinical trials. Women's Health experience is a plus! Job ...

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Clinical Research Associate Ii information

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$12

$41

$69

How much do clinical research associate ii jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for clinical research associate 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 is a clinical research associate ii?

Clinical Research Associate IIs are professionals who monitor and manage clinical trials to ensure that they are conducted in compliance with regulatory requirements and study protocols. They are responsible for overseeing the progress of clinical research at various sites, ensuring accurate data collection, and maintaining patient safety. Typically, a CRA II has more experience than an entry-level CRA, taking on additional responsibilities such as mentoring junior staff and handling more complex studies. Their work is crucial in bringing new medical treatments and devices to market.

What are the key skills and qualifications needed to thrive as a clinical research associate ii?

To thrive as a Clinical Research Associate II, you need a solid understanding of clinical trial protocols, Good Clinical Practice (GCP), and a relevant bachelor’s degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, regulatory submission processes, and certifications such as ACRP or SOCRA are commonly required. Attention to detail, effective communication, and strong organizational skills set outstanding candidates apart in this role. These competencies are crucial for ensuring compliance, data integrity, and the successful management of clinical trials.

How does a clinical research associate ii typically collaborate with investigators and study coordinators at clinical trial sites?

As a Clinical Research Associate II, you will regularly interact with investigators and study coordinators to ensure that clinical trials are conducted according to protocol, regulatory requirements, and good clinical practice (GCP) guidelines. This often involves performing site visits, providing ongoing training, resolving study-related queries, and verifying accurate data collection and documentation. Building strong professional relationships and maintaining clear communication are key, as you will serve as a primary liaison between the sponsor and site staff, helping to address challenges and keep studies on track.

What is the difference between Clinical Research Associate II vs Clinical Research Associate I?

AspectClinical Research Associate IClinical Research Associate II
Required CredentialsBachelor's degree, some certifications (e.g., CCRP optional)Same as CRA I, often with additional experience
Work EnvironmentEntry-level, supporting clinical trials under supervisionMore independent, handling complex trials
Employer & Industry UsagePharmaceutical, biotech, CROsSame as CRA I, with increased responsibilities
Common Search & ComparisonOften compared with CRA II for career progressionHigher level role with more experience required

The main difference between Clinical Research Associate II and Clinical Research Associate I lies in experience and independence. CRA II professionals typically handle more complex trials and work more independently, while CRA I roles are more supportive and entry-level. Both roles require similar educational backgrounds and certifications, but CRA II positions demand greater experience and expertise.

More about Clinical Research Associate Ii jobs

What cities are hiring for Clinical Research Associate Ii jobs?

Cities with the most Clinical Research Associate Ii job openings:

What are the most commonly searched types of Clinical Research Ii jobs?

The most popular types of Clinical Research Ii jobs are:

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Clinical Research Associate Ii jobs near you
Infographic showing various Clinical Research Associate Ii job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $85,542 per year, or $41.1 per hour.

Clinical Research Associate II / Senior Clinical Research Associate

410 ICR United States USA

Raleigh, NC • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 4 days ago

Job description

North America | Remote | Sponsor-Dedicated (FSP) Opportunities

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.


At ICON Strategic Solutions, we're continually growing our network of talented Clinical Research Associates across North America. As we expand our partnerships with leading global sponsors, we are seeking experienced CRA II and Senior CRA professionals interested in sponsor-dedicated opportunities.

About the Opportunity

As a Clinical Research Associate within our sponsor-dedicated environment, you will play a critical role in the successful delivery of clinical trials, helping bring innovative therapies to patients worldwide.

Depending on your experience level, you may:

  • Conduct site qualification, initiation, routine monitoring, and close-out visits
  • Ensure protocol compliance, patient safety, data quality, and regulatory adherence
  • Build strong relationships with investigative sites and key stakeholders
  • Identify and proactively resolve site and study issues
  • Collaborate with cross-functional teams to support successful study delivery
  • Support inspection readiness and high-quality study execution
  • Mentor and guide less experienced CRAs (Senior CRA level)

What We're Looking For

CRA II

  • Bachelor's degree in a scientific, healthcare, or related field
  • Clinical monitoring experience within the pharmaceutical, biotech, or CRO industry
  • Strong knowledge of ICH-GCP, clinical trial regulations, and monitoring practices
  • Ability to work independently while collaborating effectively across teams

Senior CRA

  • Significant clinical monitoring experience across multiple studies and sites
  • Advanced knowledge of clinical trial processes, regulations, and site management
  • Proven ability to manage priorities and drive study quality independently
  • Experience mentoring or supporting other CRAs is advantageous

For all applicants

  • Strong communication and relationship-building skills
  • Willingness to travel as required
  • Passion for advancing clinical research and improving patient outcomes

When you join ICON Strategic Solutions, you gain the best of both worlds:

  • Work within dedicated sponsor environments
  • Build expertise with leading global pharmaceutical and biotechnology companies
  • Access diverse opportunities across multiple therapeutic areas
  • Benefit from ICON's global scale, career development, and support network
  • Join a culture focused on innovation, collaboration, and patient impact
  • Competitive compensation and benefits package

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