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Full Time Icon Clinical Research Jobs (NOW HIRING)

ICON

Patient Recruitment Associate I

Statesville, NC · On-site

This role is with Accellacare, part of ICON's clinical research network, where you'll play a key ... Hours : Full-Time, 8:00am - 5:00pm, Monday through Friday What you will be doing: * Screen ...

ICON

CRC Level 1

Lombard, IL · On-site

$23.75 - $31.75/hr

Clinical Research Coordinator Level 1 - Lombard, IL (Onsite) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

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 ...

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 plc

Scientist 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

Rochester, NY · On-site

$110K - $138K/yr

Senior Clinical Research Associate- Northeast ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

ICON

Site Selection Lead

Blue Bell, PA · On-site

Site Selection Lead - United States (Remote) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

ICON

Senior Clinical Research Associate

Knoxville, TN · On-site +1

Senior Clinical Research Associate - Oncology - Knoxville, TN ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to ...

ICON

Clinical Research Associate

Clinical Research Associate - Multi TA/Oncology - US ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

ICON

Senior Clinical Research Associate

Los Angeles, CA · On-site +1

$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 ...

ICON

Senior Clinical Research Associate

Miami, FL · On-site +1

Senior Clinical Research Associate - Oncology Phase I - Miami, FL ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments ...

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Showing results 21-40

All JobsIcon Clinical Research JobsFull Time Icon Clinical Research Jobs

Full Time Icon Clinical Research information

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$49K

$107.3K

$189K

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

As of Aug 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?

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?

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Full Time Icon Clinical Research jobs near you
Infographic showing various Full Time Icon Clinical Research job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Patient Recruitment Associate I

ICON

Statesville, NC • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 14 days ago

Job description

Patient Recruitment Associate - Winston Salem, NC or Statesville, NC (Onsite Hybrid)
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 Patient Recruitment Associate (PRA) to join ICON's Accellacare team, on a 6-month contract. The PRA is integral to support the growth and success of Accellacare as an organization. The PRA will encourage patients to participate in clinical research studies, through conducting phone screens. They will review patient's basic medical information to determine eligibility, discuss research opportunities, maintain the patient database, and report recruitment outcomes.
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: Winston-Salem, NC or Statesville, NC (Onsite 4 days per week)
Contract Duration: 6 months, with eligibility to convert permanent
Hours: Full-Time, 8:00am - 5:00pm, Monday through Friday
What you will be doing:
  • Screen potential study participants accordingly to protocol inclusion and exclusion criteria by asking study specific questions
  • Review, enter, and edit patient information into clinical trial management software
  • Book patients into site schedulers ensuring that entries are accurate and up to date
  • Read and understand the purpose and inclusion/exclusion criteria for each protocol
  • Respond to all leads within a 24-hour time period
  • Identify appropriate study opportunities for interested volunteers based on knowledge of clinical trials and neighboring locations
  • Problem solve and create contingency plans to optimize enrollment
  • Effectively communicate the importance of research participation to volunteers
  • Provide an exceptional patient experience by building positive rapport and consistent follow-up
  • Strive to meet personal and team targets
  • Work in strict confidentiality in all forms including electronically, written forms, and verbal
  • Remain accountable for delivering high quality, accurate work, ensuring all administration is filed accordingly

Your profile:
  • Bachelors degree in life science, healthcare, or medical field
  • Clinical research site experience (strongly preferred) with an interest in a career clinical research, preferably in patient recruitment
  • Experience in customer service, marketing, and/or sales (preferred)
  • Basic understanding of medical terminology
  • Excellent communication and interpersonal skills with comfortability fielding inbound and outbound phone calls
  • Ability to multitask while working under pressure and with tight deadlines
  • Organizational skills with attention to detail
  • Computer skills, specifically with Microsoft Office Suite (Excel, Word, Outlook)
  • Ability to work onsite in either Statesville, NC or Winston-Salem, NC 4 days per week

#LI-TP1
#LI-Hybrid
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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