Maintain and organize clinical trial documentation
Support preparation of study materials
As a Clinical Trial Associate at ICON, you will assist with the design and analysis of clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies
Job Summary
As a Clinical Trial Associate at ICON, you will assist with the design and analysis of clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.
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 Clinical Trial Associate at ICON, you will assist with the design and analysis of clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
Skills & Requirements
Must-have
assist in coordination and administration
maintain and organize clinical trial documentation
support preparation of study materials
work with cross-functional teams
track and report clinical trial metrics
Nice-to-have
foster an inclusive environment
drive innovation and excellence
advance innovative treatments and therapies
nurture talent
focus on well-being and work life balance
Key Requirements
Bachelor's degree in scientific or healthcare field
Prior experience or strong interest in clinical research
Knowledge of clinical trial processes, regulations, and guidelines
Ability to work collaboratively in fast-paced environment
Willingness to travel as required (approximately 10%)