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 general expertise. This is a hands-on role that balances meticulous regulatory work with meaningful clinical impact.Compensaciones / Beneficios
- 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 timelinesResponsabilidades




- 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