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Internship Icon Clinical Trial Jobs in Basking Ridge, NJ

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Senior Clinical Research Associate

New York, NY

$110K - $138K/yr

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 ...

ICON

Senior CRA

New York, NY · On-site +1

$110K - $138K/yr

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 ...

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Senior CRA

Basking Ridge, NJ

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 ...

Icon plc

Senior CRA

New York, NY

$110K - $138K/yr

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 ...

Icon plc

Senior CRA

New York, NY

$110K - $138K/yr

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 ...

Icon plc

Senior CRA

New York, NY

$110K - $138K/yr

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 ...

ICON

Clinical Study Lead

Warren, NJ · On-site +1

$121K - $151K/yr

Clinical Study Lead ICON is a global healthcare intelligence and clinical research organisation ... Maintain clinical trial registry entry/updates, as required. * Provides mentorship/guidance to ...

ICON

Senior Clinical Research Associate

New York, NY · On-site +1

$110K - $138K/yr

Senior Clinical Research Associate - Oncology - New York ICON is a global healthcare intelligence ... Solid tumor clinical trial experience is required * Experience utilizing Veeva systems is highly ...

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Clinical Study Lead

Warren, NJ · Hybrid

$121K - $151K/yr

Clinical Study Lead ICON is a global healthcare intelligence and clinical research organisation ... Maintain clinical trial registry entry/updates, as required. * Provides mentorship/guidance to ...

ICON

Senior Clinical Research Associate

New York, NY · On-site +1

$110K - $138K/yr

Senior Clinical Research Associate - Oncology - Central/East (NY/NJ or TX) ICON is a global health ... Reviews and verifies accuracy of clinical trial data collected, either onsite or remotely

ICON

Clinical Study Specialist

Warren, NJ · On-site

$62K - $77K/yr

Clinical Study Specialist (Hybrid office/home based in Warren NJ, Armonk NY or Cambridge MA) ICON ... Performs scheduled reconciliations of study Trial Master File (TMF) with clinical study lead ...

410 ICR United States USA

Senior CRA

Basking Ridge, NJ · On-site

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 ...

Icon plc

Clinical Study Specialist

Warren, NJ · Hybrid

$62K - $77K/yr

Clinical Study Specialist (Hybrid office/home based in Warren NJ, Armonk NY or Cambridge MA) ICON ... Performs scheduled reconciliations of study Trial Master File (TMF) with clinical study lead ...

Icon plc

Clinical Study Specialist

Warren, NJ · Hybrid

$62K - $77K/yr

Warren, NJ, Armonk NY or Cambridge MA ICON is a global healthcare intelligence and clinical ... Performs scheduled reconciliations of study Trial Master File (TMF) with clinical study lead ...

Icon plc

Clinical Study Specialist

New York, NY · Hybrid

$62K - $77K/yr

Clinical Study Specialist (Hybrid - Warren, NJ, Armonk, NY or Cambridge MA)) ICON is a global ... Performs scheduled reconciliations of study Trial Master File (TMF) with clinical study lead ...

Icon plc

Clinical Study Specialist

Warren, NJ · Hybrid

$62K - $77K/yr

Clinical Study Specialist (Hybrid - Warren, NJ, Armonk, NY or Cambridge MA)) ICON is a global ... Performs scheduled reconciliations of study Trial Master File (TMF) with clinical study lead ...

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Senior Clinical Research Associate

New York, NY · Hybrid

$110K - $138K/yr

Senior Clinical Research Associate - Oncology - New York ICON is a global healthcare intelligence ... Act as the primary contactandfacilitateefficientcommunications between the client's clinical trial ...

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All JobsIcon Clinical Trial JobsInternship Icon Clinical Trial JobsInternship Icon Clinical Trial Jobs in Basking Ridge, NJ

Internship Icon Clinical Trial information

See Basking Ridge, NJ salary details

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

As of Aug 24, 2026, the average hourly pay for internship icon clinical trial in Basking Ridge, NJ is $38.82, according to ZipRecruiter salary data. Most workers in this role earn between $26.49 and $49.57 per hour, depending on experience, location, and employer.

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 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 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 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.

What job categories do people searching Internship Icon Clinical Trial jobs in Basking Ridge, NJ look for?

The top searched job categories for Internship Icon Clinical Trial jobs in Basking Ridge, NJ are:

What cities near Basking Ridge, NJ are hiring for Internship Icon Clinical Trial jobs?

Cities near Basking Ridge, NJ with the most Internship Icon Clinical Trial job openings:

Internship Icon Clinical Trial jobs near you

Senior Clinical Research Associate

Icon plc

New York, NY

$110K - $138K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 28 days ago

Job description

Senior Clinical Research Associate- Northeast

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 requesthere.

Salary Range

$110,520.00-$138,150.00

Are you a current ICON Employee? Please click here to apply

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