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Clinical Research Associate at ICON plc - ApplyBlast

Clinical Research Associate

ICON plc

4 months ago

Brazil

Hybrid

Full Time

Intern

0 applicants

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About this role

As a Clinical Research Associate I or II at ICON in Sâo Paulo, you will contribute to clinical trial operations by coordinating study setup and monitoring activities. You will ensure patient safety and regulatory compliance while building collaborative relationships with clinical investigators and site staff. This role involves managing sponsor queries, preparing feasibility studies, and maintaining high-quality documentation across clinical programmes.

Responsibilities

Coordinate all activities for setting up and monitoring clinical studies
Run sponsor generated queries and take responsibility for study cost efficiency
Ensure patient safety through compliance with procedures and regulatory requirements
Develop strong collaborative relationships with clinical investigators and site staff
Prepare and review study documentation for new proposals

Skills

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.