Our Mandant, an innovative biotech company in the clinical Phase 2 stage, is seeking a Clinical Trial Project Manager to oversee the execution of international clinical trials in the field of neurodegenerative and ophthalmologic diseases. Your Responsibilities Drafting and reviewing clinical trial documents, including study protocols, patient information, investigator brochures, study plans, manuals, and reports End-to-end execution of clinical trials, including comprehensive monitoring activities from study start-up through close-out Development of deviation plans; defining and assessing protocol deviations at patient, site, and study level, and recommending follow-up actions Providing clinical expertise and conducting risk/benefit assessments Oversight and management of CROs and other vendors (e.g., labs) Managing study budgets, overseeing change orders, and reviewing/approving invoices Contributing to the selection of clinical service providers Reviewing and tracking study documents for regulatory submissions Supporting audits and inspections (GCP), and contributing to CAPA development and implementation Reviewing data management documents (e.g., DMP, DVP) and biostatistics documents (e.g., SAP, TFL) Coordinating study logistics including medication, samples, materials, and managing the Trial Master File Monitoring and analyzing clinical study data Preparing and delivering internal and external presentations Conducting trainings related to study processes and procedures Supporting the development and review of SOPs Your Qualifications Degree in a life science or medical-related field Minimum 3 years of experience in conducting and managing clinical studies Proven professional experience in the biotechnology industry Solid understanding of GCP/GCLP guidelines and regulatory frameworks Experience in clinical trial budgeting and vendor selection Excellent English verbal and written communication skills - german is a plus What the Mandant Offers Fully remote work setup within Germany A role within a fast-moving and globally oriented biotech environment Direct communication structures and minimal bureaucracy Attractive performance-based bonus scheme Seniority level Associate Employment type Full-time Job function Science, Research, and Project Management Industries Biotechnology Research and Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Constares GmbH by 2x Get notified about new Clinical Trial Project Manager jobs in Germany. Cologne, North Rhine-Westphalia, Germany #J-18808-Ljbffr