Site Partner II

Clinical Careers Page(26 days ago)

RemoteFull TimeMedior$107,218 - $142,797 (estimated)Clinical Research

About this role

The Study Start Up Specialist II at ICON is responsible for coordinating all activities related to site activation and start-up processes in clinical trials. The role involves building strong site relationships, ensuring regulatory and documentation compliance, and supporting project management to deliver efficient study initiation.

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Required Skills

GCP
Regulatory Compliance
Site Coordination
Documentation
Clinical Trial Management
ICH-GCP
Risk Management
Project Coordination
Communication
Regulatory Submissions

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.

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