Global Study Manager - Vendor Mgmt experience neededICON is a integral 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 Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes.What You Will Do:Your focus will be on coordinating clinical trial management delivery, resolving issues, and developing team capability.Key responsibilities include:Budget Oversight Oversee the clinical portion of the budget to ensure efficient resource allocation.Ensuring Effective Study Oversight: Develop monitoring plans and tools, ensuring effective study oversight.Optimizing Performance: Train and mentor Clinical Research Associates (CRAs) to optimize their performance.Timely Study Start-Up & Enrollment:
Drive enrollment and lead study start-up activities, adhering to timelines.Improving Study Integrity Review trip reports and implement corrective and preventative action plans when necessary.Building Productive Relationships: Foster productive relationships with Sponsors, vendors, and cross-functional teams.Your Profile:You will have solid clinical trial management experience, with the ability to manage competing priorities and develop your team.Required qualifications and experience:A minimum of 4+ years of experience in a Clinical Trial Management position at a CRO or Pharmaceutical Organization.Bachelor's degree in health, life sciences, or other relevant fields of study.At least 10+ years of relevant experience in clinical trial management.Preferred: 2+ years of monitoring experience.Experience in managing complex or global trials is advantageous.Preferred: Experience in managing all