SP l São Paulo
Efetivo (CLT)
Administrador
Biólogo
Biomédico
Bioquímico
Biotecnologista
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.
