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 ...
Clinical Sample Processor I
Portland, OR · On-site
Clinical Sample Processor I - Portland Oregon (OR) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...
Clinical Sample Processor I
Portland, OR · On-site
Clinical Sample Processor I - Portland Oregon (OR) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...
Project Leader - Medical Communications/Publications ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...
Project Leader - Medical Communications/Publications ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...
As a Supervisor, Inventory at ICON, you will oversee the inventory management processes, ensuring accurate tracking, organization, and distribution of supplies and materials for clinical trials. What ...
As a Supervisor, Inventory at ICON, you will oversee the inventory management processes, ensuring accurate tracking, organization, and distribution of supplies and materials for clinical trials. What ...
CRA II
Portland, OR · 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 ...
CRA II
Portland, OR · 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 ...
Clinical Research Associate II
Portland, OR · On-site
$91K - $114K/yr
Clinical Research Associate - Oncology - West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...
Clinical Research Associate II
Portland, OR · On-site
$91K - $114K/yr
Clinical Research Associate - Oncology - West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...
Senior Clinical Research Associate
$110K - $138K/yr
Senior Clinical Research Associate - Oncology - West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...
Senior Clinical Research Associate
$110K - $138K/yr
Senior Clinical Research Associate - Oncology - West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...
Project Leader, Clinical Research, Full-time w/ benefits, Portland, Oregon (OR) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines ...
Project Leader, Clinical Research, Full-time w/ benefits, Portland, Oregon (OR) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines ...
(Sr) Project Manager, Feasibility Site Activation ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...
(Sr) Project Manager, Feasibility Site Activation ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...
Project Manager, Imaging and Cardiac 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 ...
Project Manager, Imaging and Cardiac 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 ...
Feasibility Informatics Manager 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 ...
Feasibility Informatics Manager 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 ...
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 ...
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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 ...
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What is ICON plc?
What are the typical responsibilities of a Clinical Research Associate at ICON plc?
What are the key skills and qualifications needed to thrive as a Clinical Research Associate at ICON plc?
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.
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Full-time
Medical, Dental, Vision, Life, Retirement
Re-posted 18 days ago
Job description
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%)
#LI-LB1 #LI-REMOTE
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