We are seeking an experienced Project Manager to join our team in Hamburg. The primary role of this position is to organize and manage clinical studies, coordinating all involved departments as well as external stakeholders, and acting as the main point of contact for the sponsor. Clinical Project Manager (m/w/d) Key Responsibilities: Setting up and conducting clinical trials in compliance with relevant local laws, regulations, and directives, ensuring adherence to scope, time, budget, and quality requirements Serving as the primary contact for sponsors Managing and overseeing all parties involved, including leading national and international project teams and handling vendor management Establishing and maintaining timelines and tracking tools Developing and maintaining trial-specific plans and manuals Implementing and maintaining risk management protocols Providing interface support for tasks such as protocol/ICF development, feasibility/site selection, EC/regulatory submission, TMF maintenance, and clinical monitoring Managing the study budget Your profile: A degree in a scientific or medical field At least 2 years of experience in clinical trial management or clinical research Experience with multicenter and ideally multinational trials is preferred Strong organizational and communication skills A well-structured, organized, and target-oriented personality, with a team-player attitude Proficiency in English Possibility of partial remote work, although some office-based work in Hamburg is preferred We look forward to receiving your application.