Central Monitor

Central Monitor ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. As a Central Monitor at ICON, you will ensure the quality and integrity of clinical trial data through centralized monitoring activities, contributing to the advancement of innovative treatments and therapies. What You Will Do: You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include:

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 from centralized monitoring activities and implement corrective and preventive actions as necessary. Utilize advanced data analytics tools and technology platforms to enhance the efficiency and effectiveness of centralized monitoring processes. Provide support and guidance to study teams on centralized monitoring methodologies, best practices, and regulatory requirements. Contribute to the development and optimization of centralized monitoring strategies and protocols to maximize data quality and compliance across clinical trials.

Your Profile: You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills. Required qualifications and experience include:

Bachelors 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 regulations). Excellent analytical and critical thinking skills with the ability to identify patterns, trends, and discrepancies in clinical trial data. Effective communication and interpersonal skills, with the ability to collaborate cross-functionally and communicate complex concepts to diverse stakeholders. Willingness to travel as required (approximately 5%)

Employment with ICON is contingent upon having the legal right to work in the country where the role is based. ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

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

Benefits may vary depending on role and location. ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.