Sie sind Experte im Bereich Medical Monitoring und ab Januar für eine neue Herausforderung verfügbar? Dann dürfte folgende Stelle bei einem internationalen Pharma-Unternehmen in München sehr interessant für Sie sein: Medical Monitor Key Responsibilities: Serve as the Medical Monitor by aiding project managers in identifying critical data risks relevant to primary objectives and offering medical insights for risk mitigation strategies. Create and update Medical Monitoring Plans. Provide medical expertise to support study teams, investigators, and sites. Offer medical input on adverse event management, including reviewing cumulative ADR/SAE listings and other emerging safety data. Review clinical data and critical study parameters. Assist the Senior Project Leader with daily logistics of assigned study tasks, including administrative duties related to study coordination. Support trial team activities such as managing trial documentation, tracking milestones, identifying and resolving issues, and escalating concerns when necessary. Participate in study meetings, organize gatherings, and coordinate internal and external communications. This may include preparing meeting agendas and minutes. Assist the Senior Project Leader in supervising CROs and other third-party vendors. Manage the Trial Master File, conduct Sponsor Quality Control of uploaded documents, and update trial-related systems (CTMS). Collaborate closely with Medical Affairs, DS Affiliates, and other functional departments at DS. Support Affiliates during the site selection process. Partner with the Senior Project Leader in budget control and forecasting. Engage in study-related interactions with healthcare professionals in Steering Committees, Data Safety Boards, and Investigator Meetings. Requirements You hold a graduate degree medical doctor (MD) or pharmacist with at least 6 years relevant clinical and scientific experience Strong experience Cardiovascular is required. Helpful if Oncology experience is available You have a strong understanding of regulatory environment (thorough knowledge of Clinical Research Principles, ICH -GCP, EU regulations governing clinical trials, standard regulatory and clinical practices and current regulatory issues related to clinical research; familiar with local regulations for non-interventional studies within EU) Knowledge of pharmaceutical business and international drug development Pro-active and self-motivated personality Excellent presentation & communication skills - combined with a strong stakeholder focus Fluent written and spoken English knowledge Haben Sie Interesse an dieser Stelle? Dann freue ich mich über Ihre E-Mail unter s.bloechl(at)progressive.de. Herzliche Grüße aus München, Stefan Blöchl Dieser Geschäftszweig der SThree GmbH betreut die ausgeschriebene Stelle im Auftrag ihres Kunden.