Clinical Development Jobs in Brazil

Minimum QualificationsDoctoral degree M.D. D.O. Ph.D. in Pharmacology or Pharm D Evidence of scholarly experience and productivity Commitment to innovative approaches to education and learning Excellent written and verbal communication skillsPreferred QualificationsExperience in teaching pharmacolog...

Job Overview:The Clinical Site Navigator role is a hybrid position that combines start-up and iHCRA/CRA responsibilities. Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical trial and potentially through closeout...

DescriptionSomos Todos InstitutoFundado em 2008 o Instituto de Responsabilidade Social Sírio-Libanês (IRSSL) nasceu com o propósito de fortalecer a atuação social voluntária da Sociedade Beneficente de Senhoras do Hospital Sírio-Libanês na saúde pública do Brasil tendo como missão levar a excelência...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionWe are currently seeking a Regulatory Affairs Specialistin Brazil to join our Regulatory Affairs department focused on local submissions. This is a fantastic opportunity to further develop your regulatory career and expertis...

Working with UsChallenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the latest breakthrou...

Job TitleRegulatory Affairs Senior Manager - Medical DevicesJob Description Blumenau SCAs Regulatory Affairs Manager for Acute Care Informatics you will lead regulatory strategy and ensure compliance for health informatics solutions and electronic medical records. Your role includes meeting global r...

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities resourcing and Functional Service (FSP) solutions....

Clinical Development Medical and Regulatory Affairs (CMR)São Paulo BrazilVocê é apaixonado por pesquisa clínica e deseja contribuir para o desenvolvimento de tratamentos que mudam vidas Se você tem sólido conhecimento em Boas Práticas Clínicas (GCP) e experiência em coordenação de ensaios clínicos...

Job Description & SummaryAt PwC our people in tax services focus on providing advice and guidance to clients on tax planning compliance and strategy. These individuals help businesses navigate complex tax regulations and optimise their tax positions.In transfer pricing at PwC you will focus on provi...

Minimum QualificationsApplicants must have an earned Ph.D. in Mechanical Engineering or a related field from an accredited university (at least conferred before the start date of September 1 2024) . Prospective candidates in all mechanical engineering areas are strongly encouraged to apply.Preferred...

SITE CONTRACT SPECIALISTPrepare negotiate and finalize agreements and budgets related to clinical trials and/or overseeing a Clinical Research Organization responsible for contract negotiations.Provide support to the clinical team in the pricing planning execution and control of site/investigator bu...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionThe Clinical Site Liaison (CSL) is a field based expert who supports the conduct and the patient recruitment of the clients global clinical trials at investigative sites through local and relational support.The successful ca...

At Gilead were creating a healthier world for all people. For more than 35 years weve tackled diseases such as HIV viral hepatitis COVID-19 and cancer working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight aga...

Your role:The Sr Manager Study Start-Up is responsible for the timely within-budget and high-quality delivery and execution of clinical study start-up and maintenance activities across the Latin America region. Reporting to the Region Head Clinical Site Management - Latin America and Puerto Rico thi...

Seu papel será:Gerenciar um portfólio de média a alta complexidade e demanda de negócios desenvolvendo as estratégias e garantindo marcos requisitos e cronogramas para fornecer aprovações regulatórias alinhadas às metas de negócios. Interações com a ANVISA e potencial posição de liderança em câmaras...

At Gilead were creating a healthier world for all people. For more than 35 years weve tackled diseases such as HIV viral hepatitis COVID-19 and cancer working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight aga...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAmendment Implementation SpecialistSummarized Purpose:Completes amendment activities within assigned projects and ensures amendment deliverables meet customer expectations as well as contracted milestones by providing accura...

Job DescriptionGeneral Summary:The Pricing & Market Access Director is responsible for leading the development and/or execution of Market Access strategies for one or more products as well as partnering cross-functionally on the Commercial and (if working at the Global / international level) Develop...