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In this role, you will coordinate and track regulatory submissions, partnering with the Regulatory Lead to prepare high-quality global submissions and ensuring timely delivery to health authorities worldwide. You will provide operational support to
Lead the full lifecycle of complex programs from contract signature to delivery. Act as the single point of contact for customers and advocate for their needs on-site. Ensure delivery on time, within budget, and to the highest quality standards.
You will oversee a team responsible for managing the end-to-end regulatory artwork process for pharmaceutical and non-pharmaceutical products across Europe. In addition to your leadership responsibilities, you’ll remain actively involved in daily
Responsible for assisting with defining compound/program medical strategies and for leading select medical affairs projects within a specific compound or indication. Support GMA the development of the Global Medical Affairs strategy and execution of the
Provision of scientific and technical leadership to multidisciplinary teams to achieve corporate goals in challenging research projects within early-stage biologics drug development; Establishing and managing research projects as project scientist;