Site engagement liaison – São Paulo/SP

Responsabilidades

• Building and maintaining strong relationships with key stakeholders at clinical trial sites, including principal investigators, site coordinators, and research staff.
• Providing support and guidance to site staff on study protocols, procedures, and regulatory requirements, ensuring compliance and successful study conduct.
• Identifying opportunities to improve site engagement and optimize site performance through regular communication and feedback mechanisms.
• Collaborating with internal teams to develop and implement site engagement strategies tailored to the specific needs of each study and site.
• Monitoring site performance metrics and providing regular updates to study teams on site engagement activities and outcomes.

Requisitos

• Bachelor’s degree in life sciences or a related field.
• Previous experience in clinical research, site management, or a related field preferred.
• Strong interpersonal and communication skills, with the ability to build rapport and establish effective working relationships with diverse stakeholders.
• Excellent organizational and problem-solving skills, with the ability to prioritize and manage multiple tasks simultaneously.
• Knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.
• Willingness to travel as required (approximately 35%).

Benefícios

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

Marcado como: Assuntos Regulatórios, Boas Práticas, Gestão de Relacionamentos, Indústria Farmacêutica, Pesquisa Clínica, Recrutamento, Saúde