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Clinical Research Associate at ICON plc - ApplyBlast

Clinical Research Associate

ICON plc

3 months ago

Blue Bell, Pennsylvania

Hybrid

Full Time

Junior

0 applicants

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About this role

An Entry Clinical Research Associate at ICON serves as the primary liaison between investigation sites and sponsors for early development multi-therapeutic clinical trials. The role involves conducting site visits, ensuring regulatory compliance, monitoring patient safety, and managing drug accountability across various therapeutic areas. Candidates must be proficient in clinical systems and capable of collaborating with cross-functional teams to drive trial success.

Responsibilities

Conduct site visits for selection, initiation, and close-out of clinical trials
Ensure site compliance with ICH-GCP and local regulatory requirements
Monitor patient safety and manage adverse event reporting
Oversee drug accountability and ensure proper storage and destruction
Support subject recruitment and retention efforts at the site level

Skills

Qualifications

Bachelor's degree in Life SciencesRegistered Nurse (RN) qualification

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.