Site qualification, initiation, monitoring, close-out
ICON plc is a world-leading healthcare intelligence and clinical research organization partnering with leading pharmaceutical organizations
Job Summary
ICON plc is a world-leading healthcare intelligence and clinical research organization partnering with leading pharmaceutical organizations.
The role involves managing clinical studies across therapeutic areas like Oncology, Neurology, Obesity, and Rare Diseases, ensuring compliance with ICH-GCP.
ICON offers comprehensive CRA development programs, competitive salaries, and a range of benefits focused on well-being and work-life balance.
Matching Summary
ICON plc is a world-leading healthcare intelligence and clinical research organization partnering with leading pharmaceutical organizations.
Skills & Requirements
Must-have
Independent monitoring Phase II-IV trials
ICH-GCP and regulatory compliance
Site qualification, initiation, monitoring, close-out
Study documentation and submissions
Cross-functional team collaboration
Patient safety assurance
Nice-to-have
Foster inclusive environment
Drive innovation and excellence
Nurture talent
Focus on well-being and work-life balance
Key Requirements
Life science degree or equivalent
2+ years independent monitoring experience (CRA II)
4+ years independent monitoring experience (Senior CRA)