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Icon Clinical Research Cra Jobs (NOW HIRING)

ICON

Clinical Research Associate

Clinical Research Associate - Multi TA/Oncology - US ICON is a global healthcare intelligence and ... Minimum of 9 months onsite monitoring experience as a Clinical Research Associate; level (CRA I ...

ICON

Clinical Research Associate

Clinical Research Associate - Multi TA/Oncology - US ICON is a global healthcare intelligence and ... Minimum of 9 months onsite monitoring experience as a Clinical Research Associate; level (CRA I ...

ICON

Clinical Research Associate II

Blue Bell, PA · On-site

CRA II or Senior CRA-US-Remote 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 ...

ICON

Clinical Research Associate

Clinical Research Associate - Multi TA ICON is a global healthcare intelligence and clinical ... As a CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial ...

ICON

CRA II

Blue Bell, PA · On-site

Senior CRA/ CRA II 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 ...

ICON

Clinical Research Associate

Long Beach, CA · On-site +1

$91K - $114K/yr

Clinical Research Associate - Early Stage Development - West Region ICON is a global healthcare ... As a CRA II at ICON, you will design and analyze clinical trials, interpreting complex medical data ...

Icon plc

CRA II

Blue Bell, PA · Remote

Senior CRA/ CRA II 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 ...

Icon plc

At ICON Strategic Solutions, we're continually growing our network of talented Clinical Research ... As we expand our partnerships with leading global sponsors, we are seeking experienced CRA II and ...

Icon plc

Clinical Research Associate II

Blue Bell, PA · Remote

CRA II or Senior CRA-US-Remote 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 ...

Icon plc

Clinical Research Associate

Washington, DC · On-site

$91K - $114K/yr

Clinical Research Associate - Early Stage Development - West Region ICON is a global healthcare ... As a CRA II at ICON, you will design and analyze clinical trials, interpreting complex medical data ...

Icon plc

Clinical Research Associate

Long Beach, CA · On-site

$91K - $114K/yr

Clinical Research Associate - Early Stage Development - West Region ICON is a global healthcare ... As a CRA II at ICON, you will design and analyze clinical trials, interpreting complex medical data ...

Icon plc

CRA II

Lawrence, KS · Remote

$91K - $114K/yr

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 ...

Icon plc

Clinical Research Associate II

Cambridge, MA · Remote

Senior CRA / CRA II - United States - Home Based ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

Icon plc

Clinical Research Associate II

Salisbury, NC · Remote

Senior CRA / CRA II - United States - Home Based ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

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Icon Clinical Research Cra information

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$11K

$79.4K

$137.5K

How much do icon clinical research cra jobs pay per year?

As of Sep 8, 2026, the average yearly pay for icon clinical research cra 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 does a Clinical Research Associate at ICON Clinical Research do?

A Clinical Research Associate (CRA) at ICON Clinical Research is responsible for monitoring clinical trials to ensure they are conducted following regulatory requirements and study protocols. CRAs act as the main point of contact between the sponsor and research sites, verifying data accuracy, ensuring participant safety, and conducting site visits. Their work is crucial in maintaining the integrity of clinical data and supporting the successful completion of clinical studies.

What are some common challenges faced by Clinical Research Associates at ICON, and how can applicants prepare for them?

Clinical Research Associates at ICON often manage multiple trials across various sites, which requires strong organizational skills and adaptability. Common challenges include ensuring compliance with complex regulatory requirements, maintaining clear communication with site staff, and managing travel schedules. Applicants can prepare by developing meticulous attention to detail, honing their time management abilities, and familiarizing themselves with Good Clinical Practice (GCP) guidelines. Building a proactive approach to problem-solving and fostering collaborative relationships with colleagues can also help navigate these challenges successfully.

What are the key skills and qualifications needed to thrive as an ICON Clinical Research CRA, and why are they important?

To thrive as an ICON Clinical Research CRA (Clinical Research Associate), you need a solid background in life sciences, clinical research processes, and regulatory guidelines, typically supported by a relevant degree and prior monitoring experience. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like GCP (Good Clinical Practice) are commonly required. Strong organizational skills, attention to detail, and effective communication make candidates excel in this role. These competencies are crucial for ensuring compliance, data integrity, and successful collaboration in complex clinical trials.

What is the difference between Icon Clinical Research Cra vs Clinical Research Associate?

AspectIcon Clinical Research CraClinical Research Associate
CertificationsTypically requires GCP training, CRA certificationRequires GCP training, often CRA certification
Work EnvironmentPharmaceutical/clinical research companies, CROsPharmaceutical companies, CROs, research sites
Employer & IndustryMajor CROs like Icon, industry-widePharmaceutical companies, CROs, industry-wide
Search & Comparison IntentIcon Clinical Research Cra vs Clinical Research AssociateSame as above

The main difference between an Icon Clinical Research Cra and a Clinical Research Associate is primarily in branding and company affiliation. Both roles involve monitoring clinical trials, ensuring compliance, and working within similar environments. The titles are often used interchangeably, but 'Icon Clinical Research Cra' specifies employment with Icon, a leading CRO, while 'Clinical Research Associate' is a broader industry term applicable across many organizations.

What are popular job titles related to Icon Clinical Research Cra jobs?

For Icon Clinical Research Cra jobs, the most frequently searched job titles are:

Infographic showing various Icon Clinical Research Cra 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 $79,437 per year, or $38.2 per hour.

Clinical Research Associate II/Sr. CRA

Detroit, MI • On-site, Remote

ICON
See more jobs at ICONexternal

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 26 days ago

Job description

CRA II/Sr. CRA- Detroit, MI
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

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