Clinical Site Associate

ICON plc

8d • Remote

About The Position

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.

Requirements

• Completed a Bachelor’s degree in a relevant field, such as Life Sciences or Healthcare.
• Minimum of one year of experience as a Study Coordinator in clinical research.
• 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
• Must have the legal right to work in the country where the role is based.

Nice To Haves

• Previous experience in clinical research or a related field preferred

Responsibilities

• 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
• Maintain Trial Master File (TMF)

Benefits

• 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

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level