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Clinical Research Associate at ICON plc - ApplyBlast

Clinical Research Associate

ICON plc

4 months ago

Sao Paulo, Brazil

Hybrid

Full Time

Junior

0 applicants

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About this role

A Clinical Research Associate at ICON executes clinical trial monitoring tasks to ensure high-quality outcomes for new medicine programs. The role involves coordinating study setup, maintaining documentation, managing sponsor queries, and ensuring regulatory compliance at clinical sites while maintaining strong relationships with investigators and staff. Candidates support study feasibility and contribute to overall clinical trial operations with a focus on patient safety and cost efficiency.

Responsibilities

Coordinate activities for setting up and monitoring clinical studies
Complete accurate study status reports and maintain documentation
Manage sponsor generated queries for cost efficiency
Ensure compliance with ICON procedures and regulatory requirements
Develop collaborative relationships with key stakeholders and investigators

Skills

Qualifications

University degree in medicine or science

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.