Support creation and management of study documents
Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders
Job Summary
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.
At ICON, inclusion & belonging are fundamental to our culture and values, and we are dedicated to providing an inclusive and accessible environment for all candidates.
Matching Summary
Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.
Skills & Requirements
Must-have
Collect, review, and track study documents
Maintain Trial Master File (TMF)
Support creation and management of study documents
Communicate with internal and external team members
Provide study metrics and reports
Nice-to-have
Foster an inclusive environment
Drive innovation and excellence
Advance innovative treatments and therapies
Grow and develop into Global Study Management
Key Requirements
Bachelor’s degree in relevant field
3+ years supporting multiple clinical studies operationally globally
Knowledge of ICH-GCP principles
Experience supporting regulatory submissions
Advanced System and IT skills (AI, eTMF, Excel, Veeva Vault, CTMS, Medidata, IMPACT, Control Room, CLIN vault)