Description
Allucent is hiring a Start-Up Associate II (SUA II) to coordinate local clinical-trial site start-up activities, including regulatory and ethical submissions, CTMS and eTMF documentation, regulatory and IEC/IRB communication, contract preparation and negotiation, site document collection, and investigational-product shipment authorization. The role requires a life-science degree or equivalent qualification, more than two years of regulatory affairs experience in pharmaceutical or biotechnology, knowledge of local submission requirements, drug-development knowledge, and fluent German and English communication skills. The position is hybrid or remote, with an in-office expectation of two days per week for employees within reasonable distance of a global office.
