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 Clinical Study Specialist role involves organizing analyzable reports, coordinating meetings, managing study documentation, tracking site activities, and supporting clinical trial operations globally.
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 committed to fostering an inclusive environment driving innovation and excellence.
Skills & Requirements
Must-have
Experience supporting global trials
Working knowledge of TMF and CTMS
Proficient in SharePoint management
Strong written and verbal communication
Self-starter with independent work capability
PowerPoint and Excel competency
Meeting coordination and minutes preparation
Nice-to-have
Vendor management and oversight experience
Solution-oriented mindset
Experience with ICF review
Process improvement initiatives
Hybrid office/home working flexibility
Key Requirements
Bachelor's Degree
Minimum 2 years industry related experience
Experience supporting global trials in NA, LAM, EU, APAC, India
Experience working with TMF, CTMS, SharePoint
Open to hybrid work in Warren NJ, Armonk NY or Cambridge MA