Job Title: Associate Director, Clinical Operations
Type: Permanent, full-time
Location: Spain, remote (you MUST be located in Spain)
Responsibilities

Lead 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 areas
Oversee CROs, vendors, and external partners to ensure high-quality delivery of clinical trial activities in compliance with ICH GxP guidelines, applicable laws and regulations.
Lead vendor selection, support contract negotiation, and ongoing vendor performance management and escalation, in collaboration with Procurement and Legal departments
Lead 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 Requirements

Proven 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.

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