Freiburg, Baden-Württemberg, Germany
Clinical research professional with hands-on experience in AMG- and MPDG-regulated clinical trials, combining site-facing study coordination with internal project management responsibilities. Currently acting as a key interface between sponsors, CROs, and investigational sites, with a strong focus on study start-up activities, regulatory submissions, and cross-functional coordination. Experienced in managing timelines, tracking study progress, and ensuring compliance within highly regulated environments. Contract and budgett responsibility‘s, main lead contract and budgett negotiatin. My therapeutic focus lies in CNS, particularly epilepsy, where I have developed a solid understanding of complex study requirements and site needs. I am especially interested in remote roles within study start-up, regulatory affairs, or clinical project management, where I can contribute to efficient study execution and high-quality delivery. Core competencies: • Study Start-Up & Regulatory (AMG/MPDG) • Cross-functional Project Coordination • Site & Stakeholder Management • Timeline & Study Tracking • CNS / Epilepsy Clinical Trials Open to opportunities as Study Start-Up Specialist/Manager, (Associate) Clinical Project Manager, or Regulatory-focused roles in clinical research.