As a Senior Regulatory Operations Associate at ICON, you will play a pivotal role in managing regulatory documents and processes, contributing to the successful execution of clinical trials and the advancement of innovative treatments and therapies
Job Summary
As a Senior Regulatory Operations Associate at ICON, you will play a pivotal role in managing regulatory documents and processes, contributing to the successful execution of clinical trials and the advancement of innovative treatments and therapies.
Oversee the preparation, compilation, and submission of regulatory documents for clinical trials, managing electronic document management systems (eTMF, eCTD) to ensure compliance and accessibility.
ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities for you and your family.
Matching Summary
As a Senior Regulatory Operations Associate at ICON, you will play a pivotal role in managing regulatory documents and processes, contributing to the successful execution of clinical trials and the advancement of innovative treatments and therapies.