Senior CRA
Lawrence, KS · On-site
As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and ...
Senior CRA
Lawrence, KS · On-site
As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
Senior CRA
New York, NY · On-site
$110K - $138K/yr
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 ...
Senior CRA
New York, NY · On-site
$110K - $138K/yr
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 ...
Senior CRA
Cambridge, MA · On-site
$110K - $138K/yr
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 ...
Senior CRA
Cambridge, MA · On-site
$110K - $138K/yr
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 ...
Senior CRA
Cambridge, MA · On-site
$110K - $138K/yr
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 ...
Senior CRA
Cambridge, MA · On-site
$110K - $138K/yr
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
Senior CRA
Kansas City, MO · On-site
As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and ...
Senior CRA
Kansas City, MO · On-site
As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and ...
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 ...
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 ...
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 ...
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 ...
Senior CRA
New York, NY · On-site
$110K - $138K/yr
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 ...
Senior CRA
New York, NY · On-site
$110K - $138K/yr
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 ...
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 ...
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 ...
Senior CRA
Blue Bell, PA · On-site
$110K - $138K/yr
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 ...
Senior CRA
Blue Bell, PA · On-site
$110K - $138K/yr
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 ...
Icon Plc information
See salary details
$19.71 - $21.77
1% of jobs
$21.77 - $23.82
1% of jobs
$23.82 - $25.87
3% of jobs
$25.87 - $27.93
6% of jobs
$27.93 - $29.98
8% of jobs
$30.59 is the 25th percentile. Wages below this are outliers.
$29.98 - $32.04
17% of jobs
The median wage is $34.01 / hr.
$32.04 - $34.09
14% of jobs
$34.09 - $36.15
19% of jobs
$37.13 is the 75th percentile. Wages above this are outliers.
$36.15 - $38.20
12% of jobs
$38.20 - $40.25
12% of jobs
$40.25 - $42.31
7% of jobs
$19
$33
$42
How much do icon plc jobs pay per hour?
As of Aug 6, 2026, the average hourly pay for icon plc in the United States is $33.79, according to ZipRecruiter salary data. Most workers in this role earn between $30.29 and $37.50 per hour, depending on experience, location, and employer.
What are the key skills and qualifications needed to thrive as a Clinical Research Associate at ICON plc?
To thrive as a Clinical Research Associate at ICON plc, you need a solid background in life sciences, clinical research experience, and often a relevant bachelor's degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is typically required. Strong organizational skills, attention to detail, and effective communication are essential soft skills for success in this role. These skills and qualifications are vital to ensuring clinical trials are conducted accurately, ethically, and in compliance with regulatory standards.
What is ICON plc?
ICON plc is a global provider of outsourced development and commercialization services to pharmaceutical, biotechnology, and medical device companies. The company specializes in clinical research and provides a wide range of services including clinical trial management, consulting, and laboratory services. ICON plc helps organizations bring new medicines and medical devices to market by managing and conducting clinical studies and ensuring regulatory compliance. Founded in 1990 and headquartered in Dublin, Ireland, ICON operates in over 40 countries worldwide.
What are the typical responsibilities of a Clinical Research Associate at ICON plc?
As a Clinical Research Associate (CRA) at ICON Plc, your primary responsibilities include monitoring clinical trial sites, ensuring compliance with study protocols, and maintaining accurate documentation. You'll frequently collaborate with site staff and cross-functional teams to resolve any issues and support patient safety and data integrity. The role requires regular travel to trial locations, attention to regulatory requirements, and effective communication skills. Your contributions are vital for keeping studies on track and ensuring high-quality, reliable results for sponsors.
What is the difference between Icon Plc vs Clinical Research Associate?
| Aspect | Icon Plc | Clinical Research Associate |
|---|---|---|
| Credentials | Typically requires a degree in life sciences, nursing, or related field; certifications like CCRA or CRA are common | Requires similar degrees; certifications like CCRA or CRA are often necessary |
| Work Environment | Global clinical trial sites, offices, and remote settings | Monitoring clinical trials at sites, coordinating with sponsors and sites |
| Employer & Industry Usage | Contract research organization (CRO) providing clinical trial services | Role within CROs, pharmaceutical companies, or biotech firms |
Icon Plc is a leading CRO that employs Clinical Research Associates (CRAs) to monitor and manage clinical trials. Both roles require similar qualifications and work in comparable environments, often within the pharmaceutical and biotech industries. The main difference lies in the company branding and specific project assignments, but their responsibilities and credentials overlap significantly.
More about Icon Plc jobs
What cities are hiring for Icon Plc jobs? Cities with the most Icon Plc job openings:
What states have the most Icon Plc jobs? States with the most job openings for Icon Plc jobs include:
What job categories do people searching Icon Plc jobs look for? The top searched job categories for Icon Plc jobs are:
Full-time
Medical, Dental, Vision, Life, Retirement
Re-posted 10 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.
We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.
What You Will Be Doing:
- 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:
- Advanced degree in a relevant field such as life sciences, nursing, or medicine.
- 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.
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver's license
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.
Are you a current ICON Employee? Please click here to apply