Job Description At Thermo Fisher Scientific, youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life enabling our customers to make the world healthier, cleaner, and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development, and delivery of life changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our D clinical research portfolio, our work spans laboratory, digital, and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on now and in the future. Location/Division Specific Information This position offers 100% remote working flexibility in Europe. Discover Impactful Work: We are seeking a highly experienced and motivated Clinical Trials Lead Programmer to join our dynamic team. In this role, you will be responsible for overseeing the statistical and programming aspects of multiple projects, acting as the lead programmer, project lead, or project oversight lead for a client/asset. You will play a crucial role in the design, analysis, and reporting of clinical trials, ensuring adherence to regulatory requirements and industry standards. Additionally, you will represent the department to clients, actively contributing to proposals and bids, and organizing teams to implement study strategies and ensure process and programming efficiencies. This position may also involve managing a small team within the programming group. A day in the Life: Serves as a lead programmer or project lead on selected studies or drug programs of all complexity and size scale. In these roles, works directly with teams and clients to conduct team meetings, develop and maintain project timelines, assess and forecast resources needed, is accountable for study budgets and familiar with any relevant contractual obligations or limits with our clients. May serve in a senior project oversight role on selected projects. May serve in a contributor or reviewer role of key submission materials for regulatory authorities. Provides general infrastructure support to the department. Exles include representing the company at industry conferences, presenting/teaching at department meetings, establishing training materials for the department, contributing to documents or policies, and contributing to process improvement and department initiatives. Increases knowledge base and professional skills for self and junior team members, in areas including programming technology and techniques, clinical trials, and developments in the pharmaceutical industry. Works to increase the visibility of the company by encouraging the publication of articles in industry journals and presentations at conferences. May manage staff of small team, w