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Full Time Icon Clinical Research Jobs (NOW HIRING)

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

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

Senior Clinical Research Associate

Chicago, IL · On-site +1

$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 ...

ICON

Senior Clinical Research Associate

Philadelphia, PA · On-site +1

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 ...

ICON

Senior Clinical Research Associate

Blue Bell, PA · On-site +1

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

Senior Clinical Research Associate

Blue Bell, PA · On-site +1

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

Senior Clinical Research Associate

Blue Bell, PA · On-site +1

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

Senior Clinical Research Associate

Los Angeles, CA · On-site +1

$110K - $138K/yr

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

ICON

Senior Clinical Research Associate

Baltimore, MD · On-site +1

Senior Clinical Research Associate - Oncology - Baltimore, MD or Phila, PA ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and ...

ICON

Senior Clinical Research Associate

Denver, CO · On-site +1

$110K - $138K/yr

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

ICON

Clinical Research Associate

Blue Bell, PA · On-site +1

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 ...

Icon plc

Sr. Clinical Research Associate

Washington, DC · On-site

$110K - $138K/yr

Senior Clinical Research Associate - Oncology (Myelofibrosis) - West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and ...

Icon plc

$110K - $138K/yr

Senior Clinical Research Associate - Oncology (Myelofibrosis) - West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and ...

ICON

Clinical Research Associate

Blue Bell, PA · On-site +1

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 ...

ICON

Senior Clinical Research Associate

Kansas City, MO · On-site +1

$110K - $138K/yr

Senior Clinical Research Associate - Cardiovascular Device - Central/West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines ...

ICON

Clinical Research Associate

Blue Bell, PA · On-site +1

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

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Showing results 21-40

All Jobsclinical research Jobsfull time 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 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:

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, 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.

Director, Clinical Research Scientist

Icon plc

Philadelphia, PA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 16 days ago

Job description

Director, Clinical Research Scientist

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.


What You Will Do:

  • Development of protocols for clinical studies.

  • Contribute to the development of program strategy for assigned compounds/programs including participation in the preparation of clinical development plans.

  • Drafting of clinical scientific documents such as IND, IND amendments, Clinical Study Reports, Investigator Brochures, Annual Reports, and other health authorities submissions.

  • Responsible for providing clinical input into eCRF design, SAP, and TLFs.

  • Monitor, review, and summarize clinical safety and efficacy data in ongoing studies.

  • Collaborate with study team members to conduct timely and thorough review of study data using best practices and available tools to identify and evaluate data trends.

  • Will lead the clinical matrix teams for assigned studies, represent clinical development on project teams and serve as liaison to project teams, CRO's and others.

  • Provide clinical updates on assigned studies to Sr. management, Project Teams, Joint Project Teams and/or Steering Committees (if appropriate), Clinical sub-teams, internal strategy, and governance meetings, eDMC meetings, steering committees, advocacy groups, scientific advisory boards, and publications committees.

  • Liaise with cross functions on training of current studies, results, meeting with lead PIs/KOLs at conferences; present as needed.

  • Develop relationships with appropriate consultants and external experts and utilize these relationships to obtain feedback on protocol design.

  • Contribute to writing and review of study abstracts, posters, oral presentations, and manuscripts for assigned studies.

Your Profile:

  • Degree in scientific/life-sciences field. Pharm.D. or Ph.D. preferred.

  • Minimum of 4 - 6 years of experience in research with at least 3 or more years of clinical research/drug development experience are required for Director level.

  • Experience in Immunology field is required.

  • Ability to multi-task and work in a fast-paced environment.

  • Excellent written and oral communication skills.

  • Strong Analytical ability.

  • Ability to accommodate up to 20% travel or as business dictates.


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

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