COMPANY OVERVIEW: Full-Life Technologies Limited ("Full-Life") is a fully integrated global radiotherapeutics company with operations in Belgium, Germany, and China. We seek to own the entire value chain for radiopharmaceutical research & development, production & commercialization in order to deliver clinical impact for patients. The Company plans to attack core issues affecting radiopharmaceuticals today through innovative research that targets the treatments of tomorrow. We are comprised of a team of fast-moving entrepreneurs and scientists with a demonstrated track record in the life sciences, as well as radioisotope research and clinical development. The team is expanding fast globally with more than 60 full-time employees now. Full-Life had completed 3 rounds of equity financing with more than $110 million raise and an acquisition with a total transaction value of $245 million in the past year. KEY RESPONSIBILITIES: Responsible for project timelines and milestones, ensuring timely completion by team members. Organize, and manage operations of a cross-functional Program Team including but not limited to Clinical Development, Clinical Operations, Regulatory Affairs, Biostatistics, Preclinical, CMC. Facilitate communication and information flow, comprising project updates, progress reports, and addressing any concerns or queries, across interdisciplinary teams and all relevant cross-functional stakeholders. Identify potential risks and assist in developing mitigation strategies to ensure successful project execution. Maintain project documentation, including project plans, schedules, budgets, and reports. Assist in monitoring project quality standards and ensuring adherence to project specifications. Preparation of internal program team meetings, including agendas, participant and speaker preparation, meeting materials, meeting management, meeting minutes and follow-up Assist with applying change, risk, and resource management. SOFT SKILLS: Outstanding organizational skills, excellent problem-solving ability and hands-on work mentality. Excellent communication and interpersonal skills Reliability and self-initiative acumen Patience and ambiguity tolerance EXPERIENCE: 1-3 years’ experience in the relevant area. Therapeutic knowledge in the areas of immunology or immuno-oncology is a must. Knowledge in radiotherapeutics is beneficial. Experience working in an international environment, especially in the USA and China, is advantageous. Experience in pharma and/or biotech industry EDUCATION: MSc/Diploma in life science or a comparable field Excellent knowledge of MS Office (Word, Power Point, Excel, One Note and MS Teams) Knowledge of program/project management software is mandatory. PMI certification will be a plus Fluency in English and German (oral and written) We look forward to seeing you