Central Review Coordinator

This is a fully remote position, open to applicants in South Africa.

📋 Description

• Perform risk evaluations on clinical trial data to pinpoint potential challenges and suggest mitigation strategies.

• Work collaboratively with cross-functional teams to create and execute risk management plans and protocols.

• Oversee data quality and integrity throughout the trial process, providing reports on findings to stakeholders.

• Employ statistical analysis and visualization tools to effectively communicate insights related to risks.

• Assist in the preparation of risk management documentation for regulatory submissions and audits.

• Deliver high-quality clinical research outputs while closely collaborating with the team and stakeholders.

⛳️ Requirements

• Bachelor's degree in statistics, life sciences, or a relevant discipline.

• Experience in clinical data analysis or risk management within a clinical research setting.

• Strong analytical capabilities with expertise in statistical software and risk assessment techniques.

• Meticulous attention to detail and a proactive mindset for identifying and managing data risks.

• Excellent communication skills, with the ability to work across diverse teams and clearly articulate complex information.

• Employment with ICON is contingent upon possessing the legal right to work in the country where the position is located.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellness programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension plans.

• Life assurance and disability coverage.

• Employee assistance programs and wellness resources.

• Opportunities for learning and development through structured training and career pathways.