Job Title:Associate Director, Clinical OperationsType:Permanent, full-timeLocation:Spain, remote (you MUST be located in Spain)ResponsibilitiesLead the strategic planning and oversight of multiple global clinical studies (Phase I–IV) in accordance with regulatory requirements, timelines, and budgets.Lead integral studies (US, Europe, LATAM, APAC) within the relevant therapeutic areasOversee CROs, vendors, and external partners to ensure high-quality delivery of clinical trial activities in compliance with ICH Gx P guidelines, applicable laws and regulations.Lead vendor selection, support contract negotiation, and ongoing vendor performance management and escalation,



in collaboration with Procurement and Legal departmentsLead program risk management to mitigate potential study specific issues. Proactive issue resolution throughout the program and lifecycle of studies, supporting the COPM..Lead and mentor Clinical Project Managers, CTAs and contractors.Further RequirementsProven track record of successfully leading global clinical trials (US, Europe, LATAM, APAC) across multiple phases and therapeutic areas.Experience in line management/oversight of Clinical Project Managers/Clinical Trial Managers.Experience in vendor/CRO selection and oversight management.Excellent leadership, communication, and organizational skills.

📌 Associate Director Clinical Operations (Madrid)
🏢 Planet Pharma
📍 Madrid