Site management associate I – São Paulo/SP [remote]

Responsabilidades

• Assisting in the monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
• Supporting site management activities, including documentation preparation, data entry, and tracking site performance metrics.
• Collaborating with cross-functional teams to facilitate communication and address site-related issues effectively.
• Maintaining accurate records of site activities and contributing to the preparation of monitoring reports.
• Participating in training and development initiatives to enhance knowledge and skills in clinical trial management.

Requisitos

• QUALIFICAÇÕES MÍNIMAS
  • Bachelor’s degree in a relevant field such as life sciences, healthcare administration, or clinical research.
  • Strong organizational skills and attention to detail, with the ability to manage multiple tasks effectively.
  • Excellent communication and interpersonal skills, with the ability to work collaboratively within a team environment.
  • Willingness to travel as required (approximately 25%).
• QUALIFICAÇÕES PREFERENCIAIS
  • Some experience in clinical research, site management, or related administrative roles.
  • Basic knowledge of clinical trial processes and regulatory requirements.

Benefícios

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

Marcado como: Biociências, Compliance, Documentação, Estudos Clínicos, Monitoramento, Pesquisa Clínica, Saúde