up study intercâmbios

Our LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, Office‑Based Regulatory Submissions Manager to join our Study Start‑Up team in Buenos Aires! This position plays a key role in the study start‑up process at Medpace. Responsibilities Efficiently manage and successfully execute all aspects of global...

Job Summary Our LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Study Start Up team in Sao Paulo! This position plays a key role in the study start up process at Medpace. If you want an exciting career where you use your previous expertise and can develop...

Summary of Responsibilities:Support the day-to-day operations of assigned activities within SSU to ensure completion per established goals and objectives in compliance with applicable GCP/ICH guidelines and other regulatory requirements. This includes effective communication and coordination with key business stakeholders (e.g., study teams) to support...

Summary of ResponsibilitiesSupport the day-to-day operations of assigned activities within SSU to ensure completion per established goals and objectives in compliance with applicable GCP/ICH guidelines and other regulatory requirements. This includes effective communication and coordination with key business stakeholders (e.g., study teams) to support timely...

Study Start Up Associate II (Supporting North America region - US/CAN) At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes...

Study Start Up Associate IIAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that...

Senior Study Start Up Associate ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and...

Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Perform tasks at a country level associated with Site...

Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.Essential FunctionsUnder general supervision, serve as...

Study Start Up Associate II (Supporting North America region - US/CAN) At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes...

About CTI CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is...

Senior Regulatory Affairs, Study Start Up Specialist CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug...

About CTI CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is...

São Paulo, Brazil Full time R1574813 Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Essential...

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.Language Requirement: Fluent English is...

O Grupo CI é Lider em edutainment, unimos educação + entretenimento,nossa missão éimpulsionar o desenvolvimento dos nossos clientes por meio da jornada de aprendizagem e experiências pelo mundo com imersão, interação e diversão.Somos um grupo sólido, com presença no Brasil e no exterior, que há mais de 35anos no mercado, proporcionando...

Assoc. Site Activation Manager (Study Start Up) – Global Study Leadership At IQVIA, our Assoc. Site Activation Managers play a critical role in bringing innovative medicines to patients faster. You'll lead global study start-up and site activation activities, partnering with sponsors, investigative sites and cross-functional teams to accelerate patient...

About Parexel Parexel is a leading global clinical development partner delivering insights-driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care...

Descrição do emprego Preparar, revisar e coordenar as submissões locais aos Comitês de Ética e autoridades regulatórias , em alinhamento com a estratégia global de submissão, desde o início do estudo até o encerramento (close-out). Demonstrar competência avançada no estabelecimento de planos de ativação do país e dos centros de pesquisa ,...

Estamos em busca de um(a) Consultor(a) Comercial Pleno para atuar no segmento de intercâmbio internacional, com foco em vendas consultivas e relacionamento com clientes. Procuramos um profissional com perfil comercial, experiência em vendas e vivência internacional, que seja organizado, proativo e orientado a resultados. A posição é 100% remota, com...