Sr clinical associate – São Paulo/SP [remote]

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

Responsabilidades

• Managing and coordinating clinical trial activities to ensure adherence to protocols, regulatory requirements, and project timelines.
• Collaborating with cross-functional teams to address clinical trial issues, optimize processes, and ensure the effective execution of studies.
• Overseeing site management and monitoring to ensure data integrity and compliance with study protocols.
• Providing guidance and support to clinical staff and investigators, ensuring adherence to best practices and regulatory standards.
• Tracking and reporting on trial progress, identifying potential risks, and implementing strategies to mitigate challenges.

Requisitos

• Bachelor’s degree in a relevant scientific discipline or healthcare-related field.
• Significant experience in clinical trial management, with a strong understanding of clinical trial processes and regulatory requirements.
• Proven ability to manage multiple projects effectively, with strong organizational and problem-solving skills.
• Excellent communication and interpersonal skills, with the ability to collaborate effectively with diverse teams and stakeholders.
• Detail-oriented with a proactive approach to ensuring trial success and addressing clinical challenges.