
10.000+ funcionários
💼 Consultoria
🏭 Manufatura
📣 Marketing
💰 $1.000.000.000 Post-IPO Debt em 2023-05
Consulting • Manufacturing • Marketing
A IQVIA é líder global em análise de dados e soluções de tecnologia, dedicada a melhorar os desfechos em saúde. A empresa utiliza sua plataforma Connected Intelligence para aproveitar o poder de analytics avançado e inteligência artificial, impulsionando a inovação na área da saúde. A IQVIA foca em diversas frentes, incluindo pesquisa clínica, tecnologia e serviços de consultoria, para solucionar desafios complexos em saúde e acelerar a entrega de novas terapias aos pacientes.
🕒 Julho 27
🗣️🇺🇸🇬🇧 Inglês obrigatório
Melhore suas chances de conseguir uma entrevista verificando sua pontuação de currículo antes de se candidatar.

10.000+ funcionários
💼 Consultoria
🏭 Manufatura
📣 Marketing
💰 $1.000.000.000 Post-IPO Debt em 2023-05
Consulting • Manufacturing • Marketing
A IQVIA é líder global em análise de dados e soluções de tecnologia, dedicada a melhorar os desfechos em saúde. A empresa utiliza sua plataforma Connected Intelligence para aproveitar o poder de analytics avançado e inteligência artificial, impulsionando a inovação na área da saúde. A IQVIA foca em diversas frentes, incluindo pesquisa clínica, tecnologia e serviços de consultoria, para solucionar desafios complexos em saúde e acelerar a entrega de novas terapias aos pacientes.
• Review of scales administered by raters in a clinical trial to ensure that assessments are being conducted in a standardized manner to ensure data reliability. • Evaluation the quality of assessments, conducting live interactions with raters to discuss assessment methodology, scoring technique, and to provide guidance, as necessary. • Evaluate case data and appropriately prepare for discussions with raters (e.g., prepared to discuss relevant issues and scale items, and have necessary documents available). • Complete rater interactions and assigned tasks as scheduled. • Responsible for timely submission of all documentation associated with assigned tasks. • Participate in all orientation, training and calibration activities as required. • Functional assessments of rater performance (e.g., mock interview) and assistance in preparing and disseminating communications. • Contacting clinical trial participants remotely (e.g., via proprietary app, Engage) to administer assessments, and will appropriately document resultant information (e.g., notes, scores)
• Minimum of a Master’s degree (MA/MS) in Psychology, Counseling, Psychiatric, Nursing or Social Work, or equivalent. • Minimum of 3 years’ clinical experience working with schizophrenia and major depressive disorder populations. • Minimum of 3 years clinical experience working administering psychiatric assessments including the PANSS, to these populations is also required. • Clinical Trials experience preferred. • Advanced level of English.
• Professional development opportunities
Candidatar-se🕒 Julho 25
Manage clinical trial operations at ICON, a global healthcare intelligence and clinical research organisation. Supporting teams to deliver high-quality outcomes across clinical programmes.
🗣️🇺🇸🇬🇧 Inglês obrigatório
🕒 Julho 21
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🗣️🇺🇸🇬🇧 Inglês obrigatório
🗣️🇪🇸 Espanhol obrigatório
🕒 Julho 14
Senior Clinical Research Associate monitoring clinical trials for the pharmaceutical industry. Conducting remote site visits and ensuring compliance with protocol and regulatory guidelines in Argentina.
🗣️🇺🇸🇬🇧 Inglês obrigatório
🕒 Julho 3
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🗣️🇺🇸🇬🇧 Inglês obrigatório
🕒 Julho 3
Clinical Trial Manager to oversee clinical operations across Latin America. Responsible for recruitment strategies and compliance in clinical studies.
🇦🇷 Argentina – Remoto
💰 $75.000.000 Private Equity Round em 2015-12
⏰ Tempo Integral
🟠 Sênior
🔴 Especialista
🧪 Pesquisa Clínica
🗣️🇺🇸🇬🇧 Inglês obrigatório