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Senior Clinical Research Associate at ICON plc - ApplyBlast

Senior Clinical Research Associate

ICON plc

4 months ago

Los Angeles, CA

Hybrid

Full Time

Senior

0 applicants

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About this role

A Senior Clinical Research Associate at ICON manages the end-to-end monitoring lifecycle for oncology clinical trials across the West region. The role involves serving as the primary liaison between investigational sites and sponsors to ensure regulatory compliance, patient safety, and data integrity. This position requires frequent travel to oversee drug accountability, conduct site visits, and maintain documentation in clinical systems.

Responsibilities

Conduct site visits for selection, initiation, routine monitoring, and close-out
Ensure site compliance with ICH-GCP guidelines and SOPs
Monitor patient safety and report adverse events accurately
Maintain up-to-date documentation in CTMS and eTMF systems
Oversee drug accountability and manage site logistics

Skills

Qualifications

Bachelor's degree in Life SciencesRegistered Nurse (RN)3+ years on-site monitoring experienceExperience monitoring Oncology or Hematology Oncology trialsProficiency in clinical systems like CTMS and eTMF

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.