ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence
Job Summary
ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence.
The role involves executing activities to fulfill sponsor oversight responsibilities, maintaining inspection-readiness, and supporting key study start-up and compliance activities.
ICON offers competitive salary and a range of benefits focused on well-being and work-life balance, including health insurance, retirement planning, and global employee assistance programs.
Matching Summary
ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence.
Skills & Requirements
Must-have
Maintain Study Inspection Readiness Tools
Coordinate TMF/Master File QC
Collaborate with CROs
Support study start-up activities
Manage compliance and quality deliverables
Nice-to-have
Team oriented and flexible
Proven collaboration and influencing skills
Ability to work independently
Interact effectively across regions and functions
Manage competing priorities
Key Requirements
Bachelor’s degree in medical or biological science or equivalent experience
Knowledge of clinical study and drug development processes
Understanding of GCP/ICH guidelines
Experience working with Clinical Research Organizations
Preferred background in medical affairs or investigator initiated studies