Job Title: Associate Director, Clinical Operations

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Type: Permanent, full-time

Location: Spain, remote (you MUST be located in Spain)

Responsibilities

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- Lead the strategic planning and oversight of multiple general clinical studies (Phase I–IV) in accordance with regulatory requirements, timelines, and budgets.

- Lead global 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

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- 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. xcskxlj

- Excellent leadership, communication, and organizational skills.

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