Study Start Up Associate I will facilitate clinical trial initiation at ICON Strategic Solutions in Buenos Aires, ensuring regulatory compliance and coordinating approvals across internal and external stakeholders to support innovative treatment development.
Responsibilities
Prepare and submit regulatory documents including clinical trial applications and ethics committee submissions
Coordinate with internal and external stakeholders to obtain necessary approvals for study initiation
Maintain accurate records of regulatory submissions and approvals
Support study teams in developing protocols, informed consent forms, and investigator brochures
Participate in study start-up meetings and advise on regulatory requirements and timelines
Requirements
Bachelor's degree in life sciences or related field
Study start-up or site activation experience in Argentina
Strong attention to detail and organizational skills
Excellent communication and interpersonal abilities
Ability to manage multiple tasks independently in fast-paced environment
Clinical research or regulatory affairs experience preferred

📌 Study Start Up Associate I (Buenos Aires)
🏢 Icon
📍 Buenos Aires