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60 Icon Clinical Trial Associate Jobs Hiring Near You

Icon plc

Senior Clinical Research Associate

Denver, CO ยท On-site

$110K - $138K/yr

Senior CRA - Colorado - Oncology ICON is a global healthcare intelligence and clinical research ... Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ...

Icon plc

$110K - $138K/yr

Senior CRA - Colorado - Oncology ICON is a global healthcare intelligence and clinical research ... Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements ...

Icon plc

West Coast Clinical Research Associate II ICON is a global healthcare intelligence and clinical ... As a CRA II at ICON Plc, you will oversee and manage clinical trial activities to ensure they are ...

ICON

Clinical Research Associate

Blue Bell, PA ยท On-site +1

Clinical Research Associate ICON is a global healthcare intelligence and clinical research ... What You Will Do: You will contribute to clinical trial monitoring activities, taking ...

ICON

Clinical Research Associate

Blue Bell, PA ยท On-site +1

Clinical Research Associate - Early Development XTA - Central ICON is a global healthcare ... What You Will Do: You will contribute to clinical trial monitoring activities, taking ...

Icon plc

Clinical Research Associate II

Cary, NC ยท Remote

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...

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Infographic showing various Clinical Trial Associate job openings at Icon in the United States as of August 2026, with employment types broken down into 99% Full Time, and 1% Part Time. Highlights an 58% Physical, 8% Hybrid, and 34% Remote job distribution.

Senior Clinical Research Associate

Icon plc

Warren, NJ

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 15 days ago

Key responsibilities

  • Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and GCP standards.

  • Conduct site visits to assess performance, resolve issues, and support successful trial execution.

  • Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting.

Job description

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 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 Be Doing:

  • 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:

  • Advanced degree in a relevant field such as life sciences, nursing, or medicine.

  • 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.

  • Must be located in the Northeast

  • Oncology monitoring experience is required

  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver's license


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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