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.
Collect, review, and track study documents, and help set up, maintain, close, and archive the Trial Master File (TMF), including regular quality checks.
ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities.
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
ICH-GCP principles knowledge
Global clinical studies operational support
Regulatory submissions experience
Advanced system and IT skills
External vendor experience
Nice-to-have
Fostering an inclusive environment
Driving innovation and excellence
Career growth into Global Study Management
Key Requirements
Bachelor’s degree in relevant field
3+ years of experience supporting multiple clinical studies operationally on a global level
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)