Support irb/ec submissions and regulatory activities
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.
As a Site Management Associate at ICON, you will play an important role in doing Study Start Up activities including trial administration, document management, regulatory support, budgeting, and meeting planning.
ICON offers competitive salary and a range of benefits focused on well-being and work-life balance, including health insurance, retirement planning, and a global employee assistance program.
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
Track essential documents and safety reports
Maintain CTMS and trackers
Support IRB/EC submissions and regulatory activities
Coordinate study tools and supplies
Organize study and investigator meetings
Nice-to-have
Strong organizational skills
Excellent communication and interpersonal skills
Ability to work collaboratively within a team environment
Attention to detail
Manage multiple tasks effectively
Key Requirements
Bachelor’s degree in life sciences or related field
2 years above solid SSU experience
Initial submission experience
Experience in clinical research or site management preferred but not mandatory