Company Description PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials
This role has a strong focus on tax technology, electronic invoicing (e-Invoicing), and statutory reporting compliance across Brazil and Latin America. The Technical Product Manager III will be responsible for driving ERP and application capabilities that
Cidade : São Paulo, Brasil Estado : São Paulo (BR-SP) País : Brasil (BR) Número da Vaga : 46310 A Data Center, Server & Storage Sr Analyst is a skilled professional responsible for the end-to-end management,
Job Description Under the oversight of the line-manager, this role is responsible for comprehensive trial and site administration and involves preparing, collating, distributing and archiving clinical documents. The CTC supports clinical supply & non-clinical supply management and
Job Title: Senior Procurement Specialist (Indirect Products) – LAM Location: Brazil (able to travel around LAM countries) Employment Type: Full-Time Job Overview We are seeking an experienced Senior Procurement Specialist to lead indirect products procurement activities
Company Description We are the company that cares - for our staff, for our clients, for our partners and for the quality of work we do. A dynamic, global company founded in 1995, we bring together
Who We Are At Kyndryl, we design, build, manage and modernize the mission-critical technology systems that the world depends on every day. So why work at Kyndryl? We are always moving forward - always pushing ourselves
Sobre Phibro Animal Health Corporation A Phibro Animal Health Corporation é uma organização de capital aberto com uma rica trajetória que abrange quase 100 anos de história. A Companhia é fabricante global de aditivos medicamentosos para
Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions - Assist Clinical Research Associates (CRAs)
Why Join Us? - Be a hero for our rare disease patients_ Our commitment and care for patients extends to our people, so culture is an essential cornerstone for Ultragenyx. We remain continuously focused on creating
Company Description NBCUniversal is one of the worlds leading media and entertainment companies. We create world-class content, which we distribute across our portfolio of film, television, and streaming, and bring to life through our theme parks
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Purpose : This position within GCSD works cross - functionally within internal (e.g. LOC) and external partners (e.g. vendors) to deliver delegated operational tasks from CSI (Commit to
Please submit your CV in English if possible, thank you! We are seeking a highly organised and motivated Digital Executive with a genuine passion for digital marketing. In this role, you will collaborate closely with our
Function - R&D Operations Sub function - Clinical Trial Support Category - Analyst, Clinical Trial Support (P4 - E24) Location - São Paulo / Brazil Date posted - Jun Requisition number - R- Work pattern -
Requisition ID: 41526 - Job Location(s): Osasco, BR Danfoss is seeking a proactive and enthusiastic Technical Assistant to establish and maintain good relationships with internal and external customers as well with service providers on behalf of
AstraZeneca is a global, innovation-driven BioPharmaceutical business that focuses on the discovery, development and commercialisation of prescription medicines for some of the worlds most serious diseases. But were more than one of the worlds leading pharmaceutical
Working with Us Challenging. Meaningful. Life-changing. Those aren’t 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.
Job Responsibilities Performs site qualification, site initiation, interim monitoring, site management activities and close‑out visits (performed on‑site or remotely) ensuring regulatory, ICH‑GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. Uses judgment and experience to evaluate
We’re expanding our capabilities across Latin America , and we’re hiring a Senior Clinical Research Associate to support critical studies across Brazil ! Responsibilities Independently oversees all aspects of study site management to ensure patient safety
Descrição da vaga Excelente porque somos plurais! Cada pessoa que compõe a BP tem uma história de vida, uma trajetória, uma visão de mundo. E ao somarmos essas visões, vemos os desafios que temos de outros