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Site Management Associate II at ICON plc - ApplyBlast

Site Management Associate II

ICON plc

4 months ago

Mexico City, Mexico

Onsite

Full Time

Junior

0 applicants

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About this role

A Site Management Associate II at ICON supports the administrative and operational management of clinical trial sites without direct on-site monitoring. The role involves ensuring compliance with Good Clinical Practice guidelines, managing Trial Master Files, and coordinating study logistics and vendor communications. This position requires collaboration across functional teams to drive study start-up, maintenance, and close-out activities effectively.

Responsibilities

Manage and maintain Trial Master File documentation quality
Support site activation by tracking essential regulatory documents
Coordinate study logistics including investigator payments and supplies
Track study progress and identify potential risks or delays
Mentor junior CTAs or administrative staff as applicable

Skills

Qualifications

Bachelor's degree in life sciencesBachelor's degree in healthcare administrationBachelor's degree in clinical research

About ICON plc

iconplc.com

Headquarters

South Dublin, Ireland

Company Size

10001+ employees

Founded

1990

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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.