Clinical Site Associate
Clinical Careers Page(1 month ago)
About this role
A Clinical Site Associate at ICON supports clinical trial operations by ensuring site compliance, accurate documentation, and readiness for audits and inspections. The role partners with Clinical Research Associates and internal teams to maintain site communications and trial master files.
Required Skills
- Site Management
- Training Coordination
- Systems Access
- Site Readiness
- Document Management
- TMF Management
- Communication
- Organization
- Attention To Detail
- Prioritization
Qualifications
- Bachelor's Degree in Life Sciences or Healthcare
About Clinical Careers Page
iconplc.comICON plc is a global clinical research organisation (CRO) that provides outsourced clinical development and commercialisation services to pharmaceutical, biotechnology and medical device companies. It offers end-to-end drug and device development support — including clinical trial management across phases, data management and biostatistics, regulatory and safety/pharmacovigilance, and commercialisation and market-access services. ICON combines scientific and therapeutic expertise with technology and a scalable global operations network to accelerate development and bring therapies to patients. Clients engage ICON for integrated, experienced CRO support across the full product lifecycle.
View more jobs at Clinical Careers Page →Apply instantly with AI
Let ApplyBlast auto-apply to jobs like this for you. Save hours on applications and land your dream job faster.
More jobs at Clinical Careers Page
Similar Jobs
Clinical Trial Assistant 2 - Sponsor Dedicated - Based in Lisbon
IQVIA(1 month ago)
TMF Reviewer III
Fortrea(1 month ago)
Clinical Trials Assistant 1
IQVIA(25 days ago)
TMF Reviewer III
Fortrea(1 month ago)
Clinical Trials Assistant (CTA) (Evergreen)
IQVIA(1 year ago)
Clinical Trials Assistant (Guangzhou)
IQVIA(2 months ago)