Clinical scientist – São Paulo/SP [remoto]

Responsabilidades

• Support the EDC transition, leveraging strong hands-on experience with Veeva EDC to ensure a smooth and effective transition.
• Apply a clinical monitoring background, ideally as a CRA and/or CTM, to support clinical study activities, data quality, and operational requirements throughout the transition.
• Designing and implementing clinical trial protocols, ensuring adherence to scientific and regulatory standards.
• Conducting data analysis and interpretation to derive insights that support study objectives.
• Collaborating with cross-functional teams to ensure effective study execution and data quality.
• Engaging with stakeholders to communicate findings and contribute to scientific discussions.

Requisitos

• Bachelor’s degree in a relevant scientific discipline or healthcare-related field.
• CRA/monitoring background with Veeva EDC experience are welcomed.
• Experience in clinical research or a related scientific role, with a strong understanding of clinical trial processes.
• Excellent analytical skills and proficiency in data interpretation and statistical analysis.
• Strong communication and collaboration skills, with the ability to work effectively in interdisciplinary teams.

Benefícios

• Various annual leave entitlements.
• Health insurance offerings.
• Retirement planning offerings.
• Global Employee Assistance Programme (LifeWorks).
• Life assurance.
• Flexible country-specific optional benefits.

Marcado como: Análise de Dados, Assuntos Regulatórios, Controle de Qualidade, Estatística, Estudos Clínicos, Indústria Farmacêutica, Pesquisa Clínica