Job Description

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise. As the world's largest FSP organization, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.Do not wait to apply after reading this description a high application volume is expected for this opportunity.Senior CRA Phase I OncologyICON is a global healthcare intelligence and clinical research organization united by a mission to bring new medicines and treatments to patients faster.As a values-driven organization, 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 CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.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:Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.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 a relevant scientific discipline or healthcare-related fieldExtensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.Willingness to travel as required (approximately 30-50%)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. xhyhwjd Benefits may include:Competitive base salary and performance related incentivesHealth and wellbeing programs including medical, dental, and vision coverage where applicableRetirement and pension plansLife assurance and disability coverageEmployee assistance programs and wellbeing resourcesLearning and development opportunities through structured training and career pathwaysBenefits may vary depending on role and location.

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