Experteer Overview
In this role you will drive site start-up activities for clinical trials, ensuring regulatory compliance and timely activation. You will collaborate with cross-functional teams and stakeholders to prepare submissions and study documents, enabling study initiation. You will contribute to advancing treatments that benefit patients through a sponsor-dedicated model and ICON’s global expertise. This is a hands-on role that balances meticulous regulatory work with meaningful clinical impact.

Compensaciones / Ventajas
• Assist in preparing and submitting regulatory documents (clinical trial applications, ethics committee submissions)
• Coordinate with internal and external stakeholders to gain approvals for study initiation
• Maintain accurate regulatory submissions and approvals records
• Support development of study documents (protocols, informed consent forms, investigator brochures)
• Participate in start-up meetings and provide input on regulatory requirements and timelines

Responsabilidades




• Bachelor in Life Sciences or related field
• Experience in submissions, substantial and non-substantial amendments Mexico
• Previous experience in clinical research or regulatory affairs preferred but not required
• Strong attention to detail and organizational skills
• Excellent communication and interpersonal skills with cross-functional collaboration
• Ability to work independently and manage multiple tasks in a fast-paced environment
• Willingness to travel ~5%

Requisitos principales
• Competitive base salary and performance-related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways

📌 Study Start Up Associate (Barcelona)
🏢 Icon Clinical
📍 Barcelona