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 you will play a pivotal role in ensuring data quality, patient safety, and study integrity across the clinical development lifecycle. What You Will Do: As a Central Monitor, you will work cross-functionally with study teams to proactively identify, assess, and mitigate risks using advanced data analytics and central monitoring tools. Key responsibilities include: Facilitate risk assessment throughout the study lifecycle, ensuring proactive identification and management of study risks Develop and maintain Central Monitoring Plans in collaboration with study teams Support study start-up, conduct, and close-out activities, including KRI (Key Risk Indicator) and QTL (Quality Tolerance Limit) definition Act as the primary point of contact for central monitoring tools and systems Review and interpret KRI/QTL outputs across sites, countries, and regions Lead and contribute to risk mitigation discussions with cross-functional stakeholders Oversee outsourced central monitoring deliverables, ensuring quality and timeliness Collaborate closely with Study Management on identified issues and trends Ensure completeness, accuracy, and compliance of Trial Master File (TMF) documentation Support continuous improvement initiatives and process enhancements within Central Monitoring Participate in vendor selection, evaluation, and oversight activities Your Profile: You are a data-driven and detail-oriented clinical professional with strong analytical capabilities and a passion for improving clinical trial quality through centralised monitoring approaches. Required qualifications and experience: BS/BA degree in biological sciences, statistics, health-related, or computer science field (advanced degree preferred) Minimum 6+ years of relevant experience, including at least 4 years in central monitoring, study management, data management, or biostatistics Demonstrated expertise in data analytics and/or monitoring across the clinical development lifecycle Experience working across multiple therapeutic areas is highly desirable Regulatory submission and audit experience Proven leadership and process improvement experience Vendor oversight and management experience Strong cross-functional knowledge of study management, data management, programming, and biostatistics Proficiency in MS Office and clinical data systems/tools Excellent communication, stakeholder management, and critical thinking skills Preferred qualifications: Professional certification in a Clinical Development discipline Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: 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. Visit our careers site to read more about the benefits ICON offers. Inclusion and Accessibility 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. ICON