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Analytical Monitor

Analytical Monitor Base - Mexico 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 Review Coordinator at ICON, you will facilitate the coordination and execution of centralized review activities for clinical trials, contributing to the advancement of innovative treatments and therapies. What You Will Do:You will take responsibility for clinical research deliverables, applying your skills to ensure quality and efficiency. Key responsibilities include:<ul><li>Coordinate the scheduling, logistics, and execution of central review activities, including imaging assessments, laboratory analyses, and other centralized evaluations.</li><li>Collaborate closely with study teams, clinical sites, and external vendors to ensure timely and accurate collection, transfer, and interpretation of clinical trial data.</li><li>Monitor the progress and quality of central review processes, proactively identifying and addressing issues or deviations to ensure adherence to protocol requirements and regulatory standards.</li><li>Maintain comprehensive documentation and records of central review activities, ensuring compliance with data management procedures and regulatory requirements.</li><li>Provide support and guidance to internal and external stakeholders on central review methodologies, protocols, and best practices.</li></ul> Your Profile:You will bring relevant clinical research experience, along with the following qualifications and skills. Required qualifications and experience:<ul><li>Bachelor's degree in life sciences, computer science, or a related discipline</li><li>Previous experience in clinical research, data management, or study coordination within the pharmaceutical, biotechnology, or CRO industry.</li><li>Strong organizational and project management skills with the ability to multitask, prioritize, and manage competing priorities in a fast-paced environment.</li><li>Excellent attention to detail and problem-solving abilities, with a commitment to ensuring data accuracy, integrity, and compliance.</li><li>Effective communication and interpersonal skills, with the ability to collaborate cross-functionally and build strong relationships with diverse stakeholders.</li></ul> Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & BenefitsICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include:<ul><li>Competitive base salary and performance related incentives</li><li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li><li>Retirement and pension plans</li><li>Life assurance and disability coverage</li><li>Employee assistance programmes and wellbeing resources</li><li>Learning and development opportunities through structured training and career pathways</li></ul> Benefits may vary depending on role and location. Visit our <a href="https://careers.iconplc.com/benefits" target="_blank" rel="noopener noreferrer">careers site</a> to read more about the benefits ICON offers. Inclusion and AccessibilityICON 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 <a href="https://careers.iconplc.com/reasonable-accommodations" target="_blank" rel="noopener noreferrer">here</a>.Are you a current ICON Employee? Please click <a href="https://wd3.myworkday.com/icon/d/task/1422$1235.htmld" target="_blank" rel="noopener noreferrer">here</a> to apply

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