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IHCRA at ICON plc - ApplyBlast

IHCRA

ICON plc

1 month ago

Paris, France

Onsite

Full Time

Medior

0 applicants

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About this role

ICON is seeking an IHCRA in Paris, France, to support the execution and management of clinical trials and contribute to the advancement of innovative treatments. The role involves overseeing clinical trial monitoring deliverables, managing contract details and site payments, and coordinating day-to-day study operations. This position requires ensuring compliance with Good Clinical Practice (GCP) and regulatory guidelines while providing training and support to site staff and investigators.

Responsibilities

Lead contract negotiation and manage site payments
Coordinate day-to-day operations of clinical studies
Ensure compliance with Good Clinical Practice guidelines

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.