The project manager II has the overall responsibility for the successful initiation, planning, execution, monitoring, controlling and closure of assigned clinical trials. The project manager II 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. Project Manager II 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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This role will be perfect for you if:

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- You want to work for a mid‑sized CRO that works on significant multisite trials, including General Phase III projects.
- You are looking to position yourself in an environment where you can grow your career alongside the company.

Client interactions

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- Serve as primary contact for the Sponsor.
- Provide efficient and timely updates on trial progress.
- Lead client calls effectively.

Project planning

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- Oversee and actively participate in the preparation of project deliverables such as study plans, protocol, informed consent form, electronic case report form (eCRF), tables/listings/figures (TLFs), clinical study report.
- Participate in the planning and conduct of the Investigator’s Meeting.
- Ensure that each site has the necessary material to adequately perform the study (e.g., investigational product, study supplies, special equipment, safety lab kits, etc.).
- Lead study start‑up activities including trial kick‑off, TMF setup, site selection and activation, vendor set‑up timelines, and site contracting and budgeting.
- Collaborate with Regulatory Affairs to ensure timely submissions and completeness of essential documents prior t

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