Clinical trial associate – São Paulo/SP [híbrido]

Responsabilidades

• Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.
• Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.
• Support the preparation of study-related materials, such as informed consent forms and case report forms.
• Work with cross-functional teams to facilitate communication and ensure smooth trial execution.
• Contribute to the tracking and reporting of clinical trial metrics and milestones.

Requisitos

• Bachelor’s degree in a scientific or healthcare-related field.
• Prior experience or strong interest in clinical research.
• Knowledge of clinical trial processes, regulations, and guidelines.
• Excellent organizational and communication skills.
• Ability to work collaboratively in a fast-paced environment with attention to detail.
• Willingness to travel as required (approximately 10%).

Benefícios

• Various annual leave entitlements.
• Health insurance.
• Retirement planning.
• Employee Assistance Programme (LifeWorks).
• Life assurance.
• Childcare vouchers.
• Bike purchase schemes.
• Discounted gym memberships.
• Subsidized travel passes.
• Health assessments.

Marcado como: Análise de Dados, Assuntos Regulatórios, Biociências, Compliance, Documentação, Estudos Clínicos, Pesquisa Clínica