Experteer Overview
Antes de solicitar este puesto, por favor, lea la siguiente información sobre esta ocasión que encontrará a continuación.
In this role you will oversee end-to-end clinical trial operations in oncology, driving high-quality outcomes across programmes. You will work with cross-functional teams and investigators to implement protocols, ensure compliance, and manage timelines, budgets, and risk. The position anchors relationships with trial sites and stakeholders while navigating regulatory and ethical guidelines. You will help shape trial design decisions and vendor selections, contributing to ICON’s mission to bring new medicines to patients faster. This role offers a hands-on, impactful opportunity in a collaborative, values-driven environment.
Compensaciones / Beneficios
• Plan and manage all aspects of clinical trials, ensuring timelines, budget, and quality standards are met
• Collaborate with cross-functional teams to implement trial protocols and procedures
• Build and maintain strong relationships with trial investigators and stakeholders
• Ensure trials comply with local, national, and international regulations and ethical guidelines
• Problem-solve and make critical decisions on trial design, vendor selection, and risk management
Responsabilidades
• University degree in medicine, science, or equivalent combination of education u0026 experience
• Demonstrated ability to drive clinical deliverables of a study
• Subject matter expertise in xqbhyrx the designated therapeutic area
• Prior monitoring experience is preferred
• Willingness to travel approximately 25%
Requisitos principales
• Competitive base salary and performance-related incentives
• Health, dental, and vision coverage
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training