← Search all jobs

Clinical Research Coordinator

ICON

Cambridge, MA · Posted October 30, 2026

Just laid off? Start here: a plan for the first weeks

See every open role at ICON

More in Massachusetts job market · All Clinical Research Coordinator jobs (274) · Pharmaceuticals & Biotech · Clinical jobs

More roles at ICON

Similar jobs

Where Cambridge, MA ranks

Where Cambridge, MA placed in our monthly rankings, month by month. Each month stays online at its own address.

Rankings about clinical jobs

Clinical jobs · Top Clinical employers · All rankings

Pay compared with the market

This listing does not state pay. Across 67 open clinical research coordinator listings that state pay, the middle half runs $64,000 to $82,000 and the median is $73,000.

Listed pay is what employers advertise, not what people are paid.

Clinical Research Coordinator salaries by state · Check your own pay

How AI is used in this kind of work

AI use among natural sciences managers is little observed so far. Measured exposure for natural sciences managers: 6% (little observed).

Share of this job’s tasks that AI is already used for at work, from real usage. It is not a forecast of job loss, and a low number means no use seen yet. Source: Anthropic Economic Index.

Check how this applies to your own job

About the job

Clinical Research Coordinator

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As an IHCRA at ICON, you will support the execution and management of clinical trials, contributing to the advancement of innovative treatments and therapies.

What You Will Do:

You will take responsibility for clinical trial monitoring deliverables, applying your skills to ensure quality and efficiency.

Key responsibilities include:

Assisting in the planning, initiation, and execution of clinical trial activities

Conducting site feasibility assessments and participating in site selection processes

Coordinating with investigative sites to ensure compliance with study protocols and regulatory requirements

Monitoring study progress and data collection activities to ensure quality and accuracy

Assisting in the preparation and review of study documentation and reports

Your Profile:

You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.

Required qualifications and experience:

Bachelor's degree in a relevant field, such as life sciences or healthcare

Previous experience in clinical research or a related field preferred

Strong organizational and communication skills

Ability to work independently and collaboratively in a fast-paced environment

Attention to detail and ability to prioritize tasks effectively

What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

Various annual leave entitlements

A range of health insurance offerings to suit you and your family’s needs.

Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.

Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.

Life assurance

Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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