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Summer Icon Clinical Research Jobs (NOW HIRING)

ICON

Sr. Clinical Research Associate

Blue Bell, PA · On-site +1

Sr. 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

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 plc

Sr Clinical Research Associate

Blue Bell, PA · On-site

Clinical Research Associate - East Coast 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 plc

Site Selection Lead

Blue Bell, PA · Remote

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

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

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

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

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 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

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 ...

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Showing results 21-40

All JobsSummer Icon Clinical Research Jobs

Summer Icon Clinical Research information

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$24

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How much do summer icon clinical research jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for summer icon clinical research in the United States is $24.09, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $24.76 per hour, depending on experience, location, and employer.

What is a Summer Icon Clinical Research position?

A Summer Icon Clinical Research position is typically an internship or temporary role offered during the summer months, where students or recent graduates work alongside experienced clinical researchers. The position involves participating in various stages of clinical trials, such as data collection, patient interaction, regulatory documentation, and analysis. These roles are designed to provide hands-on experience in clinical research, helping participants develop an understanding of clinical trial protocols, ethical considerations, and research methodologies. Summer Icon Clinical Research positions are valuable for those considering a career in medicine, pharmaceuticals, or scientific research.

What are some common challenges faced by clinical research interns during a summer program, and how can they prepare for them?

Clinical research interns in summer programs often encounter challenges such as quickly adapting to complex regulatory protocols, managing large volumes of data, and balancing multiple tasks within tight timelines. To prepare, it's helpful to review basic clinical research methodologies, develop strong organizational skills, and familiarize yourself with commonly used software like REDCap or Excel. Proactive communication with supervisors and team members can also help clarify expectations and ensure smooth collaboration throughout the internship.

What is the difference between Summer Icon Clinical Research vs Summer Icon Clinical Research Coordinator?

AspectSummer Icon Clinical ResearchSummer Icon Clinical Research Coordinator
Primary RoleAssists in clinical trial activities, data collection, and site supportManages patient recruitment, schedules, and ensures protocol adherence
Required CredentialsTypically no formal certification, relevant coursework helpfulOften requires relevant healthcare or research certifications
Work EnvironmentResearch sites, laboratories, or clinical settingsClinical sites, hospitals, or research facilities
Employer & Industry UsagePharmaceutical companies, research institutionsHospitals, clinics, research organizations

In summary, Summer Icon Clinical Research roles focus on supporting clinical trials through data and site assistance, while Summer Icon Clinical Research Coordinators take on more responsibility in managing patient interactions and trial logistics. Both roles are essential in the clinical research process but differ in scope and responsibilities.

What are the key skills and qualifications needed to thrive as a clinical research associate, and why are they important?

To thrive as a Clinical Research Associate, you need a solid understanding of clinical trial protocols, regulatory guidelines, and typically hold a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like GCP (Good Clinical Practice) are common requirements. Attention to detail, strong organizational skills, and effective communication make a candidate stand out in this role. These skills ensure accurate data collection, compliance with regulations, and successful coordination among research teams and study sites.
More about Summer Icon Clinical Research jobs
What cities are hiring for Summer Icon Clinical Research jobs? Cities with the most Summer 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 Summer Icon Clinical Research jobs? States with the most job openings for Summer Icon Clinical Research jobs include:
What job categories do people searching Summer Icon Clinical Research jobs look for? The top searched job categories for Summer Icon Clinical Research jobs are:
Summer Icon Clinical Research jobs near you
Infographic showing various Summer 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 $50,108 per year, or $24.1 per hour.

Sr. Clinical Research Associate

ICON

Blue Bell, PA • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 12 days ago

Job description

Sr. 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-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
What You Will Do:
You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.
Key responsibilities include:
  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
  • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
  • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
  • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
  • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:
You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.
Required qualifications and experience:
  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
  • Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
  • Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
  • Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
  • Willingness to travel as required (approximately 60%)

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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