This role involves leading operational activities from study start-up to close-out while ensuring compliance with Good Clinical Practices and sponsor standards
Job Summary
This role involves leading operational activities from study start-up to close-out while ensuring compliance with Good Clinical Practices and sponsor standards.
The successful candidate will compile high-quality Investigator Initiation Packages and manage regulatory submissions including FDA 1572 forms and IRB approvals.
ICON offers a competitive salary, comprehensive health insurance, retirement planning, and a global Employee Assistance Programme focused on well-being.
Matching Summary
This role involves leading operational activities from study start-up to close-out while ensuring compliance with Good Clinical Practices and sponsor standards.
Skills & Requirements
Must-have
Bachelor's degree in life sciences
2+ years clinical research experience
Knowledge of ICH-GCP guidelines
Experience with US regulatory requirements
Strong English communication skills
Nice-to-have
Process improvement initiative participation
Cross-functional team collaboration
Project management prioritization skills
Key Requirements
Bachelor's degree in life sciences or related field
Minimum 2 years experience in study start-up
Understanding of local and international regulatory requirements