Site Management Associate

Clinical Careers Page(13 days ago)

RemoteFull TimeJunior$41,628 - $56,738 (estimated)Clinical Research

About this role

The Study Delivery Specialist at ICON plc supports clinical trial site management activities, ensuring compliance with study protocols and regulatory standards. The role involves administrative, monitoring, and collaborative tasks aimed at facilitating clinical research operations. It offers an opportunity to contribute to the advancement of healthcare through clinical research support.

View Original Listing

Required Skills

Clinical Research
Site Management
GCP
Data Entry
Documentation
Regulatory Compliance
Communication
Organization
Teamwork
Healthcare

Qualifications

Bachelor’s Degree in Life Sciences, Healthcare Administration, or 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 →