Senior Central Monitor

ICON (Accellacare/PRA) Regional United States (PRA) Updated 14 September 2026
PharmaCROClinical ResearchRegulatory Affairscro

Job description

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 Senior Central Monitor at ICON, you will ensure the quality and integrity of clinical trial data through comprehensive monitoring and oversight. What You Will Do: You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. Key responsibilities include: Conducting detailed central monitoring of clinical trial data to identify and address issues related to data quality and compliance. Collaborating with clinical teams to implement strategies for data management and resolve data discrepancies. Overseeing data review processes to ensure adherence to protocols and regulatory requirements. Providing guidance and training to clinical staff on best practices for data collection and reporting. Developing and refining monitoring procedures and tools to enhance the efficiency and effectiveness of central monitoring. Your Profile: You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others. Required qualifications and experience: Bachelor's degree in life sciences, computer science, or a related discipline Extensive experience in clinical monitoring, with a strong focus on data quality and regulatory compliance. Demonstrated leadership skills with the ability to manage multiple projects and collaborate effectively with cross-functional teams. Expertise in data management and analysis, with proficiency in relevant software and monitoring tools. Excellent communication and interpersonal skills, with the ability to provide clear guidance and support to clinical teams. 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 . Are you a current ICON Employee? Please click here to apply

Stand out for this role

NoxPharm tailors your CV to this job description by aligning your experience with the role requirements and terminology. Built for pharma & life sciences.

Tailor my CV now — free to try