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Clinical Team Lead Ii

hace 2 meses


Madrid, España Rho A tiempo completo

.OverviewJoin us in redefining what it means to work for a CRO. Working at Rho, you'll be joining a team who take healthcare and clinical research personally, with shared experiences that drive a passion to heal, cure and solve some of humanity's biggest challenges.At Rho, we're committed to you just as you're committed to us. You'll have the opportunity to experience a thriving company with real stability - financial, workforce, and corporate, which has created a safe environment to innovate and develop over a long and rewarding career.With a collaborative team of smart, talented, and positive people, you'll be celebrated and respected for your expertise and given the freedom to think creatively, challenge the norm,and problem-solve.We are currently hiring a Clinical Team Lead II to join our team The Clinical Team Lead is integral to driving project success.In this role, you will have the opportunity to independently manage and lead the clinical team on select projects. You'll provide direction to and train CRAs assigned to those projects.In addition, you'll be responsible for the oversight of all operational aspects related to the planning and management of CRA and site performance.You'll ensure that sites and CRAs operate in compliance with study protocols, ICH / GCP guidelines, and local Regulations.Our Clinical Operations Team will tell you, joining Rho has been one of their best career moves in terms of contentment, financial rewards and career growth, which is why we have such stability in the groupResponsibilities- Proactively drive project success, including working closely with Project Managers to develop and implement enrollment strategiesResponsible for operational aspects of planning and management of site performance in accordance with departmental productivity expectationsDevelop monitoring tools and plansDetermine and drive the study start up process (track and report progress, review data), ensuring that all sites are selected and supplies provided in accordance with study start expectationsProvide skilled review of study protocols and other study materials (e.G