Sr. Clinical Research Associate

Clinical Careers Page(4 days ago)

PennsylvaniaOnsiteFull TimeSenior$70,000 - $90,000

About this role

A Senior Clinical Research Associate at ICON plc specializes in site monitoring activities within clinical trials, ensuring site compliance and data quality across Phase I-IV studies. The role involves managing relationships with study sites, overseeing study conduct, and supporting study teams in a dynamic and regulated environment.

View Original Listing

Required Skills

Veeva EDC
TMF
CTMS
Risk-Based Monitoring
Source Data Verification
Regulatory Compliance
Site Management
Clinical Trials
ICH GCP
Data Review

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 →