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Merck is a leading science and technology company in healthcare, life science and performance materials. Around 50,000 employees in 67 countries work to further develop technologies that improve and enhance life – from biopharmaceutical therapies to treat cancer or multiple sclerosis, cutting-edge systems for scientific research and production, to liquid crystals for smartphones and LCD televisions.
Your role:Be accountable for day to day activities of all aspects for the management of local/regional company-sponsored studies, including study plans, timelines, resources, problem identification and resolution, status reports and budget to ensure timely delivery of completed study reports to the project teams. Manage independent consultants including CROs, clinicians, independent CRAs, or statisticians when required by the project including selection, coordination of project specific training, and payment. Develop and monitor study budget and timelines. Monitor work to ensure quality. Ensures that trials are entered into the company´s Clinical Trial Management System and other systems, if applicable. Understanding of local / country requirements for areas of responsibility Managing and steering CROs successfully. Networking skills to represent Merck with key local, regional and global stakeholders. Working Experience with international operating NPOs would be desirable
Who you are
What we offer:Your possibilities to develop in our growing company are just as manifold as our product portfolio. We offer a modern and international working environment to unleash your innovative potential in diverse teams, and take responsibility for our employees, products, the environment and society.
Curious? Apply and find more information at come2merck.com