This is a talent pool for people with disabilities. If you do not belong to this group and wish to apply, you can apply for other vacancies within IQVIA jobs. Job Overview IQVIA is committed to
Visão de Trabalho Atuação estratégica em Inteligência de Mercado na indústria farmacêutica, responsável por transformar dados de mercado, epidemiológicos e competitivos em insights para tomada de decisão. Busca-se um profissional com forte capacidade analítica, conhecimento das
Location: Brazil (Sao Paulo) About Us: Join our team and help shape the future of our organization. We are a leading company committed to excellence and innovation, seeking a talented Senior Recruiter to support our growth.
Job Overview Senior Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Senior Project Lead is an essential
Location: Brazil (Sao Paulo) About Us: Join our team and help shape the future of our organization. We are a leading company committed to excellence and innovation, seeking a talented Senior Recruiter to support our growth.
Visão de Trabalho Buscamos um(a) Analista Pleno de SFE (Sales Force Effectiveness) para atuar na análise e otimização da performance comercial, transformando dados em insights estratégicos para apoiar a tomada de decisão. Será responsável pelo desenvolvimento
IQVIA Biotech is hiring for Site Contracts Associate with 1-3 years experience negotiating clinical site contracts and budget templates. IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience,
About us At ExxonMobil, our vision is to lead in energy innovations that advance modern living while reducing emissions. As one of the world’s largest publicly traded energy and chemical companies, we are powered by a
Visão da Posição Buscamos um(a) Coordenador(a) de Business Operations & Projects para atuar no suporte tático às operações e projetos da área, garantindo a eficiência dos processos administrativos, a gestão e acompanhamento de contratos, a manutenção
Job Overview Provide project related assistance to assigned project teams.; Ensure all work is conducted in accordance with standard operating procedures, policies, good clinical practices and applicable regulatory requirements.; Meeting quality and timeline metrics.; Essential Functions
Localização: Preferencialmente em regiões com fácil acesso a aeroportos e ampla conectividade aérea Modelo de atuação: Campo | Viagens frequentes Regime de contratação: CLT Sobre a oportunidade Buscamos um(a) Consultor(a) Científico(a) para atuar como referência técnico-científica
At Hologic, our purpose is to enable healthier lives, everywhere, every day. As a global leader in diagnostics and women’s health, we are driven by The Science of Sure — delivering innovative technologies that support earlier
About Us Visa is a world leader in payments technology, facilitating transactions between consumers, merchants, financial institutions and government entities across more than 200 countries and territories, dedicated to uplifting everyone, everywhere by being the best
Job overview The Pharmacovigilance Specialist will support Local Pharmacovigilance Organization on various activities related to the Global Safety Database to ensure that reporting rules are set in accordance with local regulations and any product vigilance agreements
PURPOSE The Internal Translator is responsible for linguistically and culturally interpreting the written material in a way that maintains or duplicates the structure and style of the original text while keeping the ideas and facts of
Clinical Trial Psych Rater - Portuguese Speaking Location: Remote/Virtual Hours: Estimated 10–16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to
You enjoy shaping the future of product innovation as a core leader, driving value for customers, guiding successful launches, and exceeding expectations. Join our dynamic team and make a meaningful impact by delivering high-quality products that
Job Overview Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work, budget and resources. Essential Functions
Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly? If
JOB SUMMARY: Responsible for medical data review and medical safety case processing and related safety activities. Performs review of medical data to ensure medical/scientific plausibility and to employ medical assessment and knowledge. Also, provides medical expertise