Experteer Overview In this role you lead the development, review, and oversight of informed consent documents for complex, global clinical trials.
You will collaborate with cross-functional teams to ensure consent materials meet protocol, regulatory, and sponsor requirements.
You advise on consent strategy, manage translation and documentation, and engage with sponsors, ethics committees, and regulators.
You'll create guidance and templates to drive standardisation and train junior staff.
This position offers meaningful impact in advancing patient-centric trial conduct within a values-driven culture.
Compensaciones / Beneficios
• Lead creation, review, and optimisation of global and local informed consent forms (ICFs) aligned with protocol, regulatory, and sponsor requirements
• Advise study teams on informed consent strategy and country-specific considerations for complex studies
• Oversee translation processes, version control, and documentation for consistency and traceability across regions
• Interface with sponsors, ethics committees, and regulatory bodies to address queries and negotiate consent wording
• Develop and maintain guidance,



templates, and best practices to drive standardisation and efficiency
• Provide training and mentorship to junior team members on informed consent principles, processes, and quality standards Responsabilidades
• Bachelor's degree in a relevant scientific discipline or healthcare-related field
• Significant clinical research experience with a strong focus on informed consent
• In-depth knowledge of GCP, ethical guidelines, and global regulatory expectations relating to consent
• Excellent writing and editing skills with the ability to convey complex information clearly
• Strong stakeholder management and cross-functional collaboration skills
• Proven ability to manage multiple studies with high accuracy, accountability, and initiative Requisitos principales
• Annual leave entitlements
• Health insurance offerings
• Competitive retirement planning offerings
• Global Employee Assistance Programme (LifeWorks)
• Life assurance
• Adaptable country-specific benefits

📌 Informed Consent Specialist Ii (Madrid)
🏢 Icon Clinical
📍 Madrid