ICON plc
ICON plc
Posted 3 months ago
Full Time
,
Remote OK
Smart Summary
Responsibilities
The role involves supporting clinical trial operations by ensuring site compliance and maintaining accurate documentation. Key tasks include managing site communications, coordinating trainings, and maintaining the Trial Master File.
Qualifications
You have completed a Bachelor's degree in Life Sciences or Healthcare and possess at least one year of experience as a Study Coordinator in clinical research. You are skilled in managing site communications, document management, and supporting site readiness activities.
Must Have Skills for ATS
Study Coordinator
clinical research
Trial Master File (TMF)
Site Support
Document Management
Job Description
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.
Clinical Site Associate (CSA)
Open to candidates located anywhere in the USA.
ICON is currently seeking a Clinical Site Associate (CSA) to join our diverse and dynamic team. We are looking for candidates with a minimum of one year of experience as a Study Coordinator in clinical research.
In this role, you will play a pivotal part in supporting clinical trial operations by ensuring site compliance, maintaining accurate documentation, and supporting audit and inspection readiness. The position involves close collaboration with Clinical Research Associates and cross-functional teams to ensure efficient and high-quality trial execution.
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What you will be doing
Site Support & Oversight:
Document Management:
Your profile
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:
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.
Are you a current ICON Employee? Please click here to apply
ICON plc
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