Senior CRA
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Before you apply
Salary$111k – $138k
LocationIndiana; Illinois; Missouri; Ohio
Work moderemote · United States
Typefull-time
SenioritySenior
Company size10,000+ people
PostedOct 27, 2026 · 1w ago
Verified live1d ago
At a glanceSummarised by Seekless from the posting.
Bachelor's degree in a relevant scientific discipline or healthcare-related field
Extensive experience as a Clinical Research Associate
Proven ability to manage multiple sites and projects simultaneously
Expertise in monitoring practices, data integrity, and site management
Proficiency in relevant clinical trial software and tools
Excellent communication, interpersonal, and stakeholder management skills
Oncology monitoring experience required
Willingness to travel as required (approximately 60%)
Candidates must be located in US Midwest
Employment with ICON is contingent upon having the legal right to work in the country where the role is based
Skills
clinical trial software
Benefits
Medical
Dental
Vision
Retirement plan
Life insurance
Disability insurance
Employee assistance program
Training and development
About the role
Senior CRA (Oncology - Midwest US)
About the company
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 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.
•
Oncology monitoring experience required
•
Willingness to travel as required (approximately 60%)
•
Candidates must be located in US Midwest
Legal
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 request here.
Salary Range
$110,520.00-$138,150.00
Are you a current ICON Employee? Please click here to apply