Medical Writer - Medical Writing & Healthcare Communications Lo444

.Detalles del empleoTipo de empleo: Jornada completaTurno y horario: De lunes a viernesUbicación: Barcelona, Barcelona provinciaDescripción completa del empleo:At Thermo Fisher Scientific, you'll 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 PPD 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.Discover Impactful Work:As a Medical Writer in the Medical Writing and Healthcare Communications team, you will write publications and other scientific communications for internal scientific collaborators and external biotech and pharmaceutical clients. In this position, you will draw on your interests and experience in science, communication, and project management. Your daily work will be to prepare documents that are clear, concise, compelling, scientifically accurate, and aligned with regulations, industry standards, and corporate guidance. You will go beyond simply disclosing information to producing documents that tell a story and, in the end, help improve patient care.You will need to master not only scientific writing but also project management and interpersonal communication. You will be challenged to work at a high level, but you won't be doing it alone – you will be part of, and be able to benefit from, a team of dynamic and experienced writers.A Day in the Life:On a daily basis, you will write, edit, and handle publications and other scientific communications (e.G., posters, abstracts, slide decks, white papers, and plain language summaries). You will need to work on multiple projects concurrently while remaining on time and within budget and complying with industry standards and internal processes. You will work in close collaboration with a line manager and senior reviewer, will be expected to help solve problems, and will frequently collaborate and communicate with scientists, coauthors, and other stakeholders. You will be challenged to master new study designs and clinical areas, as well as the craft of scientific writing