Role Description A Vitru Educação está em busca de professor(a)-autor(a) para atuar na revisão técnica, validação acadêmica e curadoria conceitual da disciplina UX RESEARCH, USABILIDADE E MÉTRICAS DE EXPERIÊNCIA, do curso Engenharia de Requisitos e UX Colaborativo, na modalidade pós-graduação EAD. SOBRE A ATIVIDADE: - Curadoria e validação de conteúdo - Revisão técnica de 3 temas (20 a 30 laudas cada) - Análise de atualidade conceitual, linguagem e adequação ao público - Conferência e eventual complementação de referências - Realização de ajustes diretamente no material (não apenas sugestões) - Atividades avaliativas e complementares - Validação de 3 questões de autoestudo por tema - Revisão e validação de 15 questões objetivas por tema - Validação de materiais complementares (1 estudo de caso + 10 questões) - Validação de roteiros e gravação de 3 videoaulas (10 a 15 minutos cada) EMENTA DA DISCIPLINA: - Pesquisa com usuários - Heurísticas de usabilidade - Testes A/B - Prototipação - Métricas de experiência do usuário (UX Metrics), incluindo NPS, CSAT, SUS e métricas comportamentais - Design orientado a dados e validação contínua de interfaces - Técnicas de coleta de dados: entrevistas, testes de usabilidade, card sorting, eye tracking e surveys Qualifications - Pós-graduação lato ou stricto sensu – Especialização, Mestrado ou Doutorado na área da disciplina* - Familiaridade com Google Docs e/ou Word - Organização, gestão de prazos e clareza na escrita - Experiência prévia na produção de livros ou materiais educacionais será considerada um diferencial - Graduação em Sistemas de Informação, Ciência da Computação, Engenharia de Software, Design, Psicologia, Administração ou áreas correlatas - Especialização e/ou Mestrado em Engenharia de Requisitos, UX, UX Research, Produto Digital, Interação Humano-Computador, Métodos Ágeis ou áreas afins Benefits - Atividade 100% home office - Acompanhamento especializado durante todas as etapas - Publicações com registro de ISBN - Desenvolvimento de competências autorais digitais - Visibilidade nacional e reconhecimento acadêmico Company Description A Vitru Educação é a maior instituição privada de ensino EAD do Brasil e referência nacional do ensino presencial e Medicina. Juntos como Vitru, Unicesumar e Uniasselvi, nos dedicamos ao desenvolvimento individual e coletivo. Nossa prioridade é o aprendizado, fazemos do conhecimento um estilo de vida!

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Parexel FSP is hiring for two experienced CRA's at either the CRA II or Senior CRA level to join one of a large Sponsor’s in the EU. This role is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution Some specifics about this advertised role - Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan and applicable prevailing laws, Good Clinical Practices. - Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through database lock, ensuring relevant timelines and quality deliverables are met. - Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites. - Monitor site level AEs and SAEs and collaborate with the Drug Safety Unit and follow-up with investigators sites, as needed, to bring SAE reports required information to resolution. - Serve as a point of contact for audit conduct, and drive Audit Observation CAPA development and checks, when applicable Who are Parexel Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base. We supported the trials of most of today’s top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients. You’ll be an influential member of the wider team. What we are looking for in this role For every role, we look for professionals who have the determination and courage always to put patient well-being first. That to us is working with heart. Here are a few requirements specific to this advertised role. - Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent - Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA and local country regulations - Monitoring Experience: Minimum 3.5 years relevant experience in clinical research site monitoring (preferably in Oncology) - Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases

Job Description At Citadel Securities, a leading global market maker, our team of quantitative researchers models the markets and brings trading strategies to life every day. Specifically, this team develops and tests automated quant trading strategies using sophisticated statistical techniques. You'll get to challenge the impossible in quantitative research by applying sophisticated and complex statistical techniques to financial markets, some of the most complex data sets in the world. Your Objectives - Conceptualize valuation strategies, develop, and continuously improve upon mathematical models and help translate algorithms into code - Back test and implement trading models and signals in a live trading environment - Use unconventional data sources to drive innovation - Conduct research and statistical analysis to build and refine monetization systems for trading signals Your Skills & Talents - Bachelor's or master's degree in mathematics, statistics, physics, computer science, or another highly quantitative field - Strong knowledge of probability and statistics (e.g., machine learning, time-series analysis, pattern recognition, NLP) - Prior experience working in a data driven research environment - Experience with translating mathematical models and algorithms into code (Python, R or C++) - Independent research experience - Ability to manage multiple tasks and thrive in a fast-paced team environment - Excellent analytical skills, with strong attention to detail - Strong written and verbal communication skills Opportunities available in Singapore and Hong Kong. About Citadel Securities Citadel Securities is a technology-driven, next-generation global market maker. We provide institutional and retail investors with world-class liquidity, competitive pricing and seamless front-to-back execution in a broad array of financial products. Our teams of engineers, traders and researchers harness leading-edge quantitative research and the accelerating power of compute, machine learning and AI to power our analytics and tackle the market's and our clients' most critical challenges. Together, we are forging the future of capital markets. For more information, visit citadelsecurities.com .

• Oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standard. • Lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting. • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct. • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.