Clinical Study Administrator

Clinical Careers Page(2 months ago)

HybridFull TimeJunior$52,293 - $70,679 (estimated)Clinical Research

About this role

A Clinical Trial Administrator at ICON is a member of the clinical research team supporting the conduct and delivery of clinical studies within a global healthcare intelligence organization. The role contributes to advancing innovative treatments and therapies by working with cross-functional teams in a regulated clinical research environment.

View Original Listing

Required Skills

Clinical Trials
Regulatory Compliance
Document Management
Informed Consent
Case Reports
Communication
Reporting
Organization
Teamwork
Detail-Oriented

Qualifications

Bachelor's Degree in Scientific or Healthcare-Related Field

About Clinical Careers Page

iconplc.com

ICON 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 →