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Responsibilities:
- Create and maintain Study Trackers and monitor screening deadlines.
- Review study visits and sweeps for readiness using page status and query reports.
- Monitor review progress, identify issues and risks, and report to Lead Central Review Manager.
Qualifications:
- BSc Life Science degree with solid experience in a CRO or pharmaceutical industry.
- Strong experience with data management systems such as Rave.
- Excellent attention to detail and effective time management skills.
Benefits:
- Competitive base salary and performance-related incentives.
- Health and wellbeing programmes including medical, dental, and vision coverage.
- Retirement and pension plans, life assurance, and disability coverage.
ICON
ICON is a global healthcare intelligence and clinical research organization that accelerates drug development. It is a large, values-driven organization with a focus on integrity, collaboration, agility, and inclusion.