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Icon Clinical Research Jobs (NOW HIRING)

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

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

Washington, DC · Hybrid

$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

Los Angeles, CA · 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 ...

ICON

Senior Clinical Research Associate

Chicago, IL · 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 ...

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 ...

ICON

Senior Clinical Research Associate

Blue Bell, PA · On-site

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

Senior CRA / CRA II - United States - Home Based 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 · Hybrid

$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 · Hybrid

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 · Hybrid

$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 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 ...

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Icon Clinical Research information

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$49K

$107.3K

$189K

How much do icon clinical research jobs pay per year?

As of Sep 3, 2026, the average yearly pay for 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 an Icon Clinical Research?

An ICON Clinical Research job typically involves working for ICON plc, a global provider of outsourced development and commercialization services to pharmaceutical, biotechnology, and medical device companies. Roles at ICON can range from clinical research associates and project managers to data analysts and regulatory specialists. Employees help design, manage, and monitor clinical trials to ensure they meet regulatory and ethical standards. These positions often require experience in clinical research, strong attention to detail, and adherence to Good Clinical Practice (GCP) guidelines.

What does a typical day look like for someone working at Icon Clinical Research?

A typical day at ICON Clinical Research often involves collaborating with cross-functional teams to oversee the progress of clinical trials, monitoring study data for accuracy, and ensuring all activities adhere to regulatory standards. You'll attend project meetings, communicate regularly with sponsors and investigators, and manage documentation and reporting tasks using specialized software. Depending on your specific role, you may also be responsible for site management, participant enrollment, or clinical data review. The work environment is fast-paced and supportive, offering opportunities for professional growth and advancement within the clinical research field.

What are the key skills and qualifications needed to thrive in the Icon Clinical Research position, and why are they important?

To thrive at ICON Clinical Research, you typically need a background in life sciences or a related field, experience with clinical trial processes, and strong analytical skills. Familiarity with industry-standard clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as GCP (Good Clinical Practice) are highly valued. Excellent organizational skills, attention to detail, and effective communication help you excel in a collaborative research environment. These skills are crucial to ensure regulatory compliance, data integrity, and successful execution of clinical trials.

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What cities are hiring for Icon Clinical Research jobs?

Cities with the most Icon Clinical Research job openings:

What are the most commonly searched types of Icon Clinical Research jobs?

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What states have the most Icon Clinical Research jobs?

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Icon Clinical Research jobs near you
Infographic showing various 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

Raleigh, NC • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 14 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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