Job Overview We are seeking participants for a conversational audio recording project involving natural customer support-style conversations using provided prompts and instructions. Selected participants may complete recordings individually or with a partner depending on the assignment
. Clinical Research Associate Brasília, DF, Brazil Ready to be the link between groundbreaking science and the patients who need it most? As a Clinical Research Associate at Novo Nordisk, youll be at the heart of clinical trials
Senior Pharmacovigilance 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
IQVIA Biotech is hiring for Sr. Site Contracts Associate in Brazil with 5 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
Graduate Pharmacovigilance 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
Pharmacovigilance 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
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
Department: Accounts Receivable Reports To: AR Supervisor & AR Manager Status: Full-Time Type of Work: Fully Remote Schedule: Mon-Fri, 8 AM – 4:30 PM PST Collaboration: Long-term Independent Contractor We are seeking a professional and results-driven
Job Overview: The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Sr
IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring in oncology. IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience,
CRA II (Location: Sao Paulo) Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them
Main activities and responsibilitiesSales and customer serviceManage to achieve sales goals set by the Store ManagerContribute to a top level customer service, in all aspects, to meet effectively any request of clienteleCollect, gather and analyse CRM
Sobre a vaga Título da vaga: Representante de Coleta de Dados em Campo Tipo de vaga: Regular, período integral. De segunda a sexta-feira Período do contrato: 10 dias úteis (incluindo treinamento) – Temporário Local: Rio de
Working with Us Challenging. 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.
Your Job : You’re not the person who will settle for just any role. Neither are we. Because we’re out to create Better Care for a Better World, and that takes a certain kind of person
Searching for: Associate, Client Success Operations About Us GSCF is a leading fintech company in the working capital finance space, serving some of the largest tech manufacturers globally. By funding, structuring, and servicing accounts receivables portfolios for
What the Associate II, Pharmacovigilance does at Worldwide Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific instructions. Serves
Sobre a vaga Título da vaga: Representante de Coleta de Dados em Campo Tipo de vaga: Regular, período integral. De segunda a sexta-feira Período do contrato: 10 dias úteis (incluindo treinamento) – Temporário Local: Rio de
Sobre a vagaTítulo da vaga: Representante de Coleta de Dados em CampoTipo de vaga: Regular, período integral. De segunda a sexta-feiraPeríodo do contrato: 10 dias úteis (incluindo treinamento) – TemporárioLocal: Rio de Janeiro, BrasilDescrição da vaga:A
Clinical Research Associate (CRA) São Paulo, Brazil Full Time Job Overvie wWe are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful execution of clinical trials. In