Central Monitor

About the role

ICON is a global healthcare intelligence and clinical research organisation seeking a Central Monitor to ensure the quality and integrity of clinical trial data through centralized monitoring activities.

Key responsibilities

• Conduct remote review and analysis of clinical trial data to identify trends, anomalies, and potential risks to patient safety and data quality.
• Collaborate with site personnel and clinical teams to address findings and implement corrective and preventive actions.
• Utilize advanced data analytics tools and technology platforms to enhance the efficiency of monitoring processes.
• Provide guidance to study teams on centralized monitoring methodologies, best practices, and regulatory requirements.

Required profile

• Bachelor's degree in life sciences, computer science, or a related discipline.
• Previous experience in clinical research, data management, or monitoring within the pharmaceutical, biotechnology, or CRO industry.
• Strong understanding of clinical trial processes, regulations, and guidelines (e.g., ICH GCP, FDA).
• Excellent analytical and critical thinking skills with the ability to identify patterns and discrepancies in data.
• Effective communication and interpersonal skills for cross‑functional collaboration.

What we offer

• Competitive base salary and performance‑related incentives.
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable.
• Retirement and pension plans, life assurance and disability coverage.
• Employee assistance programmes and wellbeing resources.
• Learning and development opportunities through structured training and career pathways.