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Internship Icon Clinical Trial Jobs (NOW HIRING)

ICON

Clinical Trial Manager

Raleigh, NC · On-site +1

Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As ...

New

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Clinical Trial Manager

Raleigh, NC

Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As ...

New

Icon plc

Clinical Trial Manager

Houston, TX · On-site

Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As ...

New

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Clinical Trial Manager

Philadelphia, PA · On-site

Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As ...

New

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Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As ...

ICON

Clinical Trial Liaison

Blue Bell, PA · On-site +1

$110K - $138K/yr

Clinical Trial Liaison 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 ...

ICON

Clinical Trial Liaison

Blue Bell, PA · On-site +1

$110K - $138K/yr

Clinical Trial Liaison 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 ...

ICON

Clinical Trial Liaison

Blue Bell, PA · On-site +1

$110K - $138K/yr

Clinical Trial Liaison - Mid- Atlantic 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 ...

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Clinical Trial Liaison

Blue Bell, PA · On-site

$110K - $138K/yr

Clinical Trial Liaison - Mid- Atlantic 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

Clinical Trial Liaison

Blue Bell, PA

$110K - $138K/yr

Clinical Trial Liaison 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 ...

ICON

Clinical Trial Liaison

Los Angeles, CA · On-site +1

$110K - $138K/yr

Clinical Trial Liaison 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 ...

ICON

Clinical Trial Liaison

Oklahoma City, OK · On-site +1

Clinical Trial Liaison 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 ...

Icon plc

Clinical Trial Liaison

Blue Bell, PA · On-site

$110K - $138K/yr

Clinical Trial Liaison 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 ...

Icon plc

Clinical Trial Liaison

New Orleans, LA · On-site

Clinical Trial Liaison 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 ...

Icon plc

Clinical Trial Liaison

Miami, FL · On-site

Clinical Trial Liaison 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 ...

Icon plc

Clinical Trial Liaison

Oklahoma City, OK · On-site

Clinical Trial Liaison 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 ...

Icon plc

Clinical Trial Liaison

Orlando, FL · On-site

Clinical Trial Liaison 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 ...

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Clinical Trial Liaison

Jacksonville, FL · On-site

Clinical Trial Liaison 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 ...

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Clinical Trial Liaison

Tampa, FL · On-site

Clinical Trial Liaison 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 ...

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Clinical Trial Liaison

Los Angeles, CA · On-site

$110K - $138K/yr

Clinical Trial Liaison 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 ...

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How much do internship icon clinical trial jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for internship icon clinical trial in the United States is $37.67, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $48.08 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an intern at ICON Clinical Trial?

To thrive as an intern at ICON in clinical trials, you typically need a background in life sciences or related fields, strong analytical skills, and an interest in clinical research. Familiarity with clinical trial management systems (CTMS), Microsoft Office Suite, and basic understanding of Good Clinical Practice (GCP) guidelines are beneficial. Excellent communication, attention to detail, and teamwork help interns effectively support projects and interact with multidisciplinary teams. These skills and qualifications are important to ensure accurate data handling, regulatory compliance, and smooth trial operations.

What types of projects and tasks can I expect to work on during an internship at ICON Clinical Trial?

As an intern at ICON Clinical Trial, you can expect to support various phases of clinical research studies, such as data management, protocol review, and regulatory documentation. Interns often collaborate with project teams, assist in preparing study materials, and help coordinate communication between departments. This role provides a hands-on introduction to clinical trial operations, offering exposure to industry-standard practices and processes. You will also gain valuable experience working alongside experienced professionals, which can serve as a strong foundation for a future career in clinical research.

What is an internship at ICON Clinical Trial?

An Internship at ICON Clinical Trial is a temporary, structured program designed for students or recent graduates interested in gaining hands-on experience in clinical research and drug development. Interns work alongside experienced professionals, assisting with various aspects of clinical trials such as data management, regulatory compliance, and patient recruitment. The internship provides valuable industry exposure, networking opportunities, and the chance to develop practical skills relevant to a career in clinical research. These programs often last several weeks to a few months, depending on the specific position and department.

What is the difference between Internship Icon Clinical Trial vs Clinical Research Coordinator?

AspectInternship Icon Clinical TrialClinical Research Coordinator
CredentialsTypically pursuing or recent graduate, no required certificationsOften requires a bachelor's degree, certifications like CCRP or CCRC preferred
Work EnvironmentInternship setting, learning-focused, temporaryFull-time, clinical trial sites, more responsibility
Employer & IndustryPharmaceutical companies, CROs, research institutionsHospitals, research centers, pharmaceutical companies

Internship Icon Clinical Trial roles are primarily learning positions for students or recent graduates gaining exposure to clinical trials. Clinical Research Coordinators are experienced professionals managing ongoing trials, requiring more credentials and responsibility. Both roles operate within the clinical research industry but differ in experience level and job scope.

More about Internship Icon Clinical Trial jobs
What cities are hiring for Internship Icon Clinical Trial jobs? Cities with the most Internship Icon Clinical Trial job openings:
What are the most commonly searched types of Icon Clinical Trial jobs? The most popular types of Icon Clinical Trial jobs are:
What states have the most Internship Icon Clinical Trial jobs? States with the most job openings for Internship Icon Clinical Trial jobs include:
What job categories do people searching Internship Icon Clinical Trial jobs look for? The top searched job categories for Internship Icon Clinical Trial jobs are:
Internship Icon Clinical Trial jobs near you
Infographic showing various Internship Icon Clinical Trial job openings in the United States as of August 2026, with employment types broken down into 83% Full Time, and 17% Part Time. Highlights an 33% In-person, 17% Hybrid, and 50% Remote job distribution, with an average salary of $78,347 per year, or $37.7 per hour.

Clinical Trial Manager

ICON

Raleigh, NC • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 3 days ago

New

Job description

Clinical Trial Manager - Phase I oncology
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 be doing
  • Manage the day-to-day operations of assigned trials and responsibilities to ensure completion per established project team goals and objectives in compliance with applicable GCP/ICH guidelines and other regulatory requirements
  • Leads or supports cross-functional trial teams, including vendors
  • Ensures accurate and up-to-date trial information within relevant tracking systems and provide regular updates of trial progression to Clinical Operations Lead, Clinical Trial Lead, and other defined stakeholders
  • Proactively identify and resolve issues that arise during trial conduct; manage escalation of trial-related issues
  • Participate in or lead the development of core trial documents, trial plans and system set-up; participate in preparation and ensure operational excellence of protocol and implementation of appropriate systems, standards, and processes to ensure quality across investigative sites, vendors, and data
  • Participate in or lead preparation of vendor requirements and project scope and selection of trial vendors; effectively manage interactions and escalations with vendor trial team
  • Participate in or lead feasibility assessment and selection of countries and sites for trial conduct
  • Participate in or facilitates site engagement and communications with investigators and/or staff to support trial milestones and deliverables
  • Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top line results; participate in data reviews and review of statistical analysis plans
  • Participate in or lead set-up and implementation of effective investigator and site monitor training; coordinate operational and therapeutic area training for internal and external trial team members
  • Provide oversight and direction to trial team members for trial deliverables
  • Manage clinical trial budget and associated vendor contracts, including tracking and data in associated systems
  • Ensure quality and completeness of TMF for assigned clinical trials
  • Participates in inspection readiness activities including coordination of clinical trial team deliverables
  • Participate in the evaluation and implementation of patient-focused strategies for assigned trials, as applicable
  • Responsible for the management of budgets, timelines and resources for assigned clinical trial responsibilities

Your profile
  • BA/BS degree with at least 3 years clinical trial experience or advanced degree (MS/PhD/PharmD) with at least 2 years clinical trial management experience
  • Must have strong knowledge of ICH/GCP guidelines and regulatory requirements
  • Must have knowledge of protocol and clinical drug development processes, clinical trial design, trial planning and management, and monitoring
  • Requires project management skills and trial leadership ability
  • Must have excellent interpersonal, written and verbal communication skills, administrative skills and computer ability
  • Fluent in English
  • Experience in Phase I oncology
  • Global experience with primary focus on independent vendor set up and management, oncology cohort management and experience in supporting dose escalation safety meetings.
  • May be asked to Work East coast hours if located further West
  • Moderate (~25%) travel required

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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