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Full Time Icon Clinical Research Jobs (NOW HIRING)

ICON

Clinical Research Nurse

Raleigh, NC · On-site

Clinical Research Coordinator Nurse - Raleigh, NC (Onsite) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

ICON

Clinical Research Nurse I

Lenexa, KS · On-site

Lenexa, Kansas (KS) Full Time, Day Shift - 10 & 12-hour shifts available, 40-hour/week. Are you a ... Join ICON as a Clinical Research Nurse , where your work supports scientific progress and helps ...

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Clinical Research Nurse

Raleigh, NC

Clinical Research Coordinator Nurse - Raleigh, NC (Onsite) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

ICON

Clinical Research Nurse

Statesville, NC · On-site

Clinical Research Nurse - Statesville, NC (Onsite) 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 Nurse

Statesville, NC · On-site

Clinical Research Nurse - Statesville, NC (Onsite) 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 Nurse I

Lenexa, KS · On-site

Lenexa, Kansas (KS) Full Time, Day Shift - 10 & 12-hour shifts available, 40-hour/week. Are you a ... Join ICON as a Clinical Research Nurse , where your work supports scientific progress and helps ...

Icon plc

Clinical Research Nurse

Piedmont, CA

Clinical Research Nurse - Statesville, NC (Onsite) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

ICON

Clinical Research Coordinator Level 1

Lombard, IL · On-site

$23.75 - $31.75/hr

Clinical Research Coordinator - Lombard, IL (Onsite) 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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Clinical Research Coordinator Level 1

Lombard, IL

$23.75 - $31.75/hr

Clinical Research Coordinator - Lombard, IL (Onsite) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

ICON

Team Lead, Site Operations

Hickory, NC · On-site

This role is with Accellacare, part of ICON's clinical research network, where you'll play a key ... Location: Full-Time Onsite at Accellacare of Hickory (221 13th Avenue Place NW Suite 201, Hickory ...

ICON

Team Lead, Site Operations (Oncology)

Lisle, IL · On-site

$68K - $85K/yr

This role is with Accellacare, part of ICON's clinical research network, where you'll play a key role in transforming the clinical trial experience for patients and sponsors alike. Our global site ...

Icon plc

Team Lead, Site Operations

Hickory, NC

This role is with Accellacare, part of ICON's clinical research network, where you'll play a key ... Location: Full-Time Onsite at Accellacare of Hickory (221 13th Avenue Place NW Suite 201, Hickory ...

Icon plc

Team Lead, Site Operations (Oncology)

Lisle, IL · On-site

$68K - $85K/yr

This role is with Accellacare, part of ICON's clinical research network, where you'll play a key role in transforming the clinical trial experience for patients and sponsors alike. Our global site ...

ICON

Lab Analyst II

Lenexa, KS · On-site

Lenexa, KS- Full Time 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

Senior Clinical Research Associate

Blue Bell, PA · On-site

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 ...

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Showing results 1-20

All JobsIcon Clinical Research JobsFull Time Icon Clinical Research Jobs

Full Time Icon Clinical Research information

See salary details

$49K

$107.3K

$189K

How much do full time icon clinical research jobs pay per year?

As of Jun 15, 2026, the average yearly pay for full time icon clinical research in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What is a Full Time ICON Clinical Research position?

A Full Time ICON Clinical Research position refers to a full-time job at ICON plc, a global contract research organization that provides outsourced development and commercialization services to the pharmaceutical, biotechnology, and medical device industries. Employees in these roles may work on clinical trials, data management, regulatory affairs, or project management to help bring new treatments to market. Full-time positions typically offer standard benefits and require a regular workweek commitment. These roles are essential for ensuring that clinical studies are conducted ethically, efficiently, and in compliance with regulatory standards.

What is the difference between Full Time Icon Clinical Research vs Full Time Clinical Research Coordinator?

AspectFull Time Icon Clinical ResearchFull Time Clinical Research Coordinator
CredentialsBachelor's degree in life sciences or related field; certifications like CCRPBachelor's degree; often certifications like CCRP or CCRC preferred
Work EnvironmentPharmaceutical companies, CROs, hospitalsResearch sites, hospitals, clinics
Employer & IndustryPharmaceutical, biotech, CROsResearch sites, hospitals, academic institutions
Common Search & ComparisonYesYes

Full Time Icon Clinical Research roles typically involve working within pharmaceutical companies or CROs, focusing on clinical trial management and data analysis. Full Time Clinical Research Coordinators usually work directly at research sites or hospitals, managing patient visits and data collection. Both roles require similar educational backgrounds and certifications, but differ mainly in work environment and specific responsibilities.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate at ICON, and why are they important?

To thrive as a Clinical Research Associate (CRA) at ICON, you need a degree in life sciences or a related field, thorough knowledge of Good Clinical Practice (GCP), and experience in clinical trial monitoring. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and regulatory documentation is essential, along with certifications such as ACRP or SOCRA being advantageous. Strong organizational skills, attention to detail, excellent communication, and the ability to manage multiple priorities help CRAs excel. These skills ensure that clinical trials are conducted safely, ethically, and efficiently while maintaining data integrity and regulatory compliance.

How does working as a full-time employee at ICON Clinical Research typically involve collaboration with cross-functional teams?

As a full-time professional at ICON Clinical Research, you can expect to work closely with a variety of cross-functional teams including clinical operations, data management, regulatory affairs, and biostatistics. Collaboration is central to the role, as projects often require input and coordination across these departments to ensure clinical trials meet regulatory standards and client expectations. Regular meetings, both in-person and virtual, are common to align on project goals and timelines. This collaborative environment fosters learning and professional growth while contributing to the overall success of each study.
More about Full Time Icon Clinical Research jobs
What cities are hiring for Full Time Icon Clinical Research jobs? Cities with the most Full Time Icon Clinical Research job openings:
What are the most commonly searched types of Icon Clinical Research jobs? The most popular types of Icon Clinical Research jobs are:
What states have the most Full Time Icon Clinical Research jobs? States with the most job openings for Full Time Icon Clinical Research jobs include:
What job categories do people searching Full Time Icon Clinical Research jobs look for? The top searched job categories for Full Time Icon Clinical Research jobs are:
Full Time Icon Clinical Research jobs near you
Infographic showing various Full Time Icon Clinical Research job openings in the United States as of June 2026, with employment types broken down into 98% Full Time, and 2% Part Time. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.
Clinical Research Nurse

Clinical Research Nurse

ICON

Raleigh, NC • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 26 days ago

Job description

Clinical Research Coordinator Nurse - Raleigh, NC (Onsite)
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 have an incredible opportunity for a Clinical Research Coordinator Nurse (CRC Nurse) to join ICON's Accellacare team. The CRC Nurse is responsible for completing trial assignments in an autonomous, accurate, and timely manner. The CRC Nurse is performing technical and clinical requirements of study protocols as ordered by the investigator.
This role is with Accellacare, part of ICON's clinical research network, where you'll play a key role in transforming the clinical trial experience for patients and sponsors alike. Our global site network is designed with one goal in mind: to deliver better access, greater efficiency, and improved outcomes in clinical research.
Location: 100% Onsite at Accellacare (3700 Barrett Drive, Suite 310 Raleigh, NC 27609)
Hours: Monday-Friday, 8:00am - 5:00pm (no weekends or holidays)
What you will be doing:
  • Coordinating and conducting clinical trial procedures according to protocol requirements
  • Performing technical and clinical requirements of study protocols, i.e., venipuncture, specimen processing, vital signs, electrocardiograms, IV infusions, IV pump operations, Holtor monitoring, pulmonary function testing, allergy testing, urine/serum pregnancy testing, strep throat screening, injections (IM or SQ) or any procedure necessary for the protocol as ordered by the investigator
  • Collecting and documenting patient data accurately and efficiently
  • Assisting in patient recruitment, screening, and enrollment processes
  • Providing nursing care and support to trial participants
  • Collaborating with interdisciplinary teams to ensure trial compliance and quality data collection

Your profile:
  • Bachelor's degree in Nursing or equivalent qualification
  • LPN required, RN preferred
  • Prior experience in clinical research coordination (preferred)
  • Strong understanding of GCP guidelines and regulatory requirements
  • Excellent communication skills
  • Organizational skills with attention to detail
  • Problem-solving skills

#LI-Onsite
#LI-TP1
#LI-Accellacare
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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