The Project Manager II, EPTR has the overall responsibility for the successful initiation, planning, execution, monitoring, controlling and closure of assigned clinical trials. The Project Manager II, EPTR oversees and coordinates study resources to ensure compliance with the study budget, project scope and timelines and in accordance with applicable standard operating procedures (SOPs), good clinical practices, regulatory and study-specific requirements. The Project Manager II, EPTR acts as the main line of communication to relevant stakeholders and provides input to feasibility, study design, budget development and ensures progress reporting (resources, budget and timeline).

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More specifically

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- Acts as the main point of contact for sponsors, vendors, and internal study teams throughout the lifecycle of a clinical trial.




- Works closely with clients at study start-up to understand their goals and help determine the most effective operational approach.
- Maintains regular communication with sponsors, study teams, functional departments, clinical sites, and senior management.
- Oversees all operational aspects of clinical trials, including timelines, budgets, resources, vendor management, and clinical operations activities, while coordinating deliverables across departments.
- Monitors and controls study budgets by tracking hours, reviewing billed time, identifying out-of-scope activities, and supporting change order management.
- Provides regular updates to internal and external stakeholders on study progress, including site selection, vendor management, budgets, timelines, quality standards, and risk mitigation efforts.
- Leads study start-up activities, including kick-off meetings, Trial Master File (TMF) setup, site selection and activation, vendor onboarding, site contracting, and budget negotiations.
- Identi

📌 Project Manager II, Early Phase (Madrid)
🏢 Indero (formerly Innovaderm)
📍 Madrid