ICON plc is a world-leading healthcare intelligence and clinical research organization committed to shaping the future of clinical development
Job Summary
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to shaping the future of clinical development.
The role involves supporting site activation by collecting, reviewing, and assembling regulatory submission packages, ensuring compliance with ICH/GCP and local regulations.
ICON offers a competitive salary and a range of benefits designed for well-being and work-life balance, including health insurance, retirement planning, and employee assistance programs.
Matching Summary
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to shaping the future of clinical development.
Skills & Requirements
Must-have
ICON SOPs/WPs knowledge
ICH/GCP knowledge
Country regulations/guidelines
Regulatory submission packages
Critical Document Package assembly
Trial Master File QC review
Nice-to-have
Inclusive environment fostering innovation
Collaboration and partnership focus
Proactive risk identification and mitigation
Commitment to ownership values
Key Requirements
Proficient knowledge of ICON SOPs/WPs
Proficient knowledge of ICH/GCP
Proficient knowledge of applicable country regulations/guidelines
Proficient in timely and accurate progress data entry