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Clinical Research Associate at ICON plc - ApplyBlast

Clinical Research Associate

ICON plc

4 months ago

Tennessee

Hybrid

Full Time

Senior

0 applicants

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About this role

This role requires an Oncology Clinical Research Associate to serve as the primary liaison between investigational sites and the sponsor, conducting site visits from selection to close-out alongside routine monitoring tasks. Candidates must ensure regulatory compliance with ICH-GCP standards while managing patient safety reporting, drug accountability, and trial documentation within CTMS and eTMF systems.

Responsibilities

Conduct comprehensive site visits including initiation and close-out
Ensure strict adherence to ICH-GCP guidelines and SOPs at clinical sites
Monitor patient safety and manage accurate adverse event reporting
Maintain rigorous documentation and resolve complex data queries
Oversee investigational drug accountability and storage protocols

Skills

Qualifications

BS in Life SciencesRN Certification2+ Years Clinical Research Experience

About ICON plc

iconplc.com

Headquarters

South Dublin, Ireland

Company Size

10001+ employees

Founded

1990

View Profile

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.