Clinical Research Coordinator

ICON Strategic Solutions; Cambridge (MA); On-site; USD 70,000 - 100,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Job summary

ICON Strategic Solutions seeks an IHCRA to support the execution and management of clinical trials. This role focuses on delivering monitoring deliverables, ensuring quality, and contributing to patient-focused treatment development.

You will coordinate with investigative sites, assist in feasibility and site selection, and help ensure regulatory adherence while thriving in a sponsor-dedicated model that leverages ICON’s global expertise.

Qualifications

• Bachelor’s degree in life sciences or healthcare.
• Experience in clinical research or related field preferred.
• Strong organizational and communication skills.
• Able to work independently and with others in a fast-paced environment.
• Attention to detail and prioritization abilities.

Responsibilities

• Monitor clinical trial deliverables to ensure quality and efficiency.
• Assist in planning, initiation, and execution of trial activities.
• Conduct site feasibility assessments and participate in site selection.
• Coordinate with investigative sites to ensure protocol and regulatory compliance.
• Monitor study progress and data collection for quality and accuracy.
• Support preparation and review of study documentation and reports.

Skills

Organization

Communication

Independent work

Prioritization

Attention to detail

Education

Bachelor’s degree in life sciences or healthcare

Tools

None

Job description

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