ZipRecruiter

Log In

2

Full Time Icon Clinical Research Jobs (NOW HIRING)

Icon plc

Clinical Research Nurse

Piedmont, CA · 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

Senior Clinical Research Associate

Blue Bell, PA · On-site

ICON plc is seeking an experienced Senior Clinical Research Associate (Senior CRA) or Clinical Research Associate (CRA) to join our dynamic, collaborative team. In this role, you will be a key ...

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

Senior Clinical Research Associate

Houston, TX · Hybrid

Contract Senior Clinical Research Associate - Home-Based (US) 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 +1

$110K - $138K/yr

Senior Clinical Research Associate 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 ...

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 plc

Senior Clinical Research Associate

Boston, MA

$110K - $138K/yr

Senior Clinical Research Associate - Oncology - East Coast 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

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

Senior Clinical Research Associate

Washington, DC · On-site +1

$110K - $138K/yr

Senior Clinical Research Associate - Oncology - Washington DC 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 - Baltimore, MD/Philadelphia, PA ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment ...

next page

Showing results 1-20

All 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 Jul 5, 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
Clinical Research Nurse

Clinical Research Nurse

Icon plc

Piedmont, CA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 17 days ago

Job description

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 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 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 Piedmont Clinic (138 Sherlock Drive, Statesville, NC, 28625)

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, 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 requesthere.

Are you a current ICON Employee? Please click here to apply

Apply