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.This role is for upcoming future opportunities that may arise at Fortrea. 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 documentsReview 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 equivalentThorough understanding of GCP, ICH Guidelines and Country regulatory environmentStrong 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 initiativesAbility of critical thinking and risk analysisFluency 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 environmentJoin 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 .
Kontaktperson:
Pharmiweb HR Team