ICON plc is a world-leading healthcare intelligence and clinical research organization committed to fostering an inclusive environment driving innovation and excellence
Job Summary
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to fostering an inclusive environment driving innovation and excellence.
The Associate Director is accountable for oversight of all assigned studies within the country, ensuring adherence to quality, timelines, and budget while driving diversity in clinical trial enrollment.
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 committed to fostering an inclusive environment driving innovation and excellence.
Skills & Requirements
Must-have
Clinical trial operations management
Global clinical trial execution
Site feasibility and monitoring
Diversity recruitment strategies
Cross-functional collaboration
Regulatory and compliance oversight
Budget and invoice management
Nice-to-have
Leadership and supervisory skills
Problem-solving and organizational skills
Effective communication abilities
Proactive issue identification
Ability to work independently
Experience with oncology and hematology trials
Travel flexibility up to 20%
Key Requirements
Bachelor’s degree
5-7 years clinical trial operations experience
3 years primary responsibility in clinical trial management
Experience in pharmaceutical/biotech or CRO
Direct management and supervisory experience
Proficient in Outlook, Word, Excel, PowerPoint
Ability to travel domestically and internationally up to 20%