Are you a dynamic leader passionate about driving clinical trials to success? We are looking for an experienced Clinical Trial Manager responsible for study oversight and delivery management (time, budget, quality)from start-up to closure in Germany. In this role, you'll collaborate with sponsors, investigators and cross-functional teams to bring life-changing treatments to patients. Key Responsibilities: Manage clinical trial activities from start-up to close-out, ensuring adherence to timelines, budgets and quality standards. Serve as the primary liaison between sponsors, sites, and internal teams, ensuring seamless communication and issue resolution. Prepare and participate in Investigator Meetings and prepare material for Site Initiation Visits. Validate study related materials (i.e. protocol, ICF, patient material) and prepare country specific documents Review Site Monitoring visit reports and ensures timelines are met. Manage site relationships (includes CRO related issues) Required Qualifications: Bachelor's or Master's degree required, preferably within Life Sciences or equivalent Thorough understanding of GCP, ICH Guidelines and Country regulatory environment Strong understanding of the clinical landscape and of clinical research processes, regulations and methodology Experience in leading or participating as an active member of cross functional teams, task forces, or local and global initiatives Ability of critical thinking and risk analysis Fluency in German and in English What We Offer: Work with an industry-leading sponsor and expand your leadership capabilities. Hybrid option (50% client-office based) and a strong focus on work-life balance. Ongoing training, leadership programs and supportive work environment Join us in advancing groundbreaking clinical research. Apply today and be part of a team that makes a difference! LI-GQ1 LI-Hybrid Learn more about our EEO & Accommodations request here .