As a Study Start Up Associate I at ICON, you will play a pivotal role in facilitating the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies
Job Summary
As a Study Start Up Associate I at ICON, you will play a pivotal role in facilitating the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies.
Coordinating with internal and external stakeholders to obtain necessary approvals and authorizations for study initiation.
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
Matching Summary
As a Study Start Up Associate I at ICON, you will play a pivotal role in facilitating the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies.
Skills & Requirements
Must-have
regulatory document preparation
stakeholder coordination
record maintenance
study document support
regulatory requirements input
Nice-to-have
inclusive environment
foster innovation
work life balance
team culture
Key Requirements
Bachelor's degree in life sciences
Previous experience in clinical research preferred
Previous experience in regulatory affairs preferred