About this role
Job title: Clinical Site Associate
About the Role ICON is seeking a Clinical Site Associate (CSA) to join our diverse and dynamic team. This remote role supports clinical trial operations across the USA, focusing on site compliance, documentation, and readiness to drive high-quality trial execution in collaboration with Clinical Research Associates and cross-functional teams.
What You'll Do
- Site Support & Oversight: Manage site-level communications; coordinate site trainings and systems access; support site readiness activities including pre/post site visit tasks; follow-up on action items.
- Document Management: Maintain Trial Master File (TMF).
What We're Looking For
- A Bachelor's degree in Life Sciences or Healthcare.
- Minimum of one year of experience as a Study Coordinator in clinical research (required).
- Previous experience in clinical research or 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.
Compensation & Benefits
- Competitive salary in USD, plus a range of benefits.
- Various annual leave entitlements.
- Health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings.
- Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of specialists for well-being support.
- Life assurance and flexible country-specific optional benefits (e.g., childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments).