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Full Time Icon Clinical Research Jobs (NOW HIRING)

Senior Clinical Research Associate - Cardio (Smartpulse A-fib) - All Regions ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and ...

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 values ...

Senior Clinical Research Associate

Portland, OR ยท On-site

$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 ...

Clinical Research Associate

Long Beach, CA ยท On-site +1

$91K - $114K/yr

Clinical Research Associate - Early Stage Development - West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and ...

Senior Clinical Research Associate

Phoenix, AZ ยท On-site

$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

Denver, CO ยท On-site

$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 - Oncology - Ohio 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 - Oncology - Jacksonville, FL ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments ...

CRA II or Senior CRA-US-Remote 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 ...

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

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 ...

Senior CRA - Northeast region (Philadelphia to Boston 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

Chicago, IL ยท Hybrid

$110K - $138K/yr

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

Senior Clinical Research Associate

Seattle, WA ยท On-site

$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 ...

Showing results 41-60

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 Sep 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 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.

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.

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:

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, 71% Full Time, 18% 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.

Senior Clinical Research Associate

ICON

Atlanta, GA โ€ข On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 4 days ago


Job description

Senior Clinical Research Associate - Cardio (Smartpulse A-fib) - All Regions
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.
To support 1study in the cardiovascular/electrophysiology medical device space. Indication is A-fib.
  • The ideal candidate will have cardiovascular medical device monitoring experience- however, complex experience in cardiovascular/electrophysiology pharma monitoring and/or Coordinator/Nursing experience will be considered.

3 years of monitoring experience required.
A bachelor's degree is required, preferably a Bachelor of Science Degree in Life Science, Physical Science, Nursing or Biological Science.
Candidates must have/ be:
  • In-depth knowledge of FDA regulations and ICH/GCP guidelines.
  • Strong problem-solving skills to mitigate risks and identify issues at sites and implement effective solutions promptly.
  • Strong interpersonal skills to establish and maintain effective working relationships with site personnel, investigators, and internal teams.
  • Exceptional verbal and written communication skills, with the ability to convey complex information clearly and concisely.
  • Ability to tailor communication style to the needs and preferences of different stakeholders, fostering a collaborative environment.
  • Ability to work independently and manage multiple priorities in a dynamic environment.
  • A well-executed plan for communication with the study teams and sites.
  • Well-versed in clinical trial management. They are rigorous, detail-oriented, and precise in their reports.
  • Located in the US near a major airport. Ability to cover up to 65% regional travel.

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