You will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies
Job Summary
You will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
Provide administrative and operational support to the Study Start-Up team, with a primary focus on regulatory document management and submission dossier preparation.
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
You will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
Skills & Requirements
Must-have
regulatory document management
submission dossier preparation
ICH-GCP adherence
essential document verification
CTMS record maintenance
Nice-to-have
foster an inclusive environment
continuous improvement culture
work collaboratively
attention to detail
Key Requirements
Bachelor's degree in scientific or healthcare field