Clinical Research Coordinator
- Location
- Cambridge, MA
- Listed
- 3 days ago
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
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.
Salary Range $56,704.00-$70,880.00
Are you a current ICON Employee? Please click here to apply
About ICON
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.
Equal opportunity and legal notices
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.
From ICON's careers page, first listed on Rolev.ai on November 6, 2026. Rolev.ai is not the employer.
How Rolev.ai helps with this application
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Common questions
Where is the Clinical Research Coordinator job at ICON located?
This Clinical Research Coordinator position at ICON is located in Cambridge, MA. Always check ICON's application page for specific state eligibility or relocation policies.
How do I apply for the Clinical Research Coordinator position at ICON?
This listing links directly to ICON's Workday application page. You can apply directly on ICON's site, or use Rolev.ai to check your resume fit, generate a zero-hallucination tailored resume and cover letter for this posting, and autofill the Workday application form in 1 click with the Rolev.ai Chrome extension. You always review the form and press Submit yourself.