- Project planning and milestone tracking
- Trial Master File (TMF) management
- Risk assessment and mitigation strategies
- Contract and site management
- Site qualification, feasibility & selection
- Supervision of vendors and subcontractors
- Budget and quality monitoring
- Remuneration and site payment management
- Management of medicinal products, medical devices and laboratory samples

Coordinating Complexity—Delivering Results
- At Alcedis, our Clinical Project Managers are more than just coordinators—they are strategic drivers of success. They lead multi-disciplinary teams across departments, manage complex timelines and budgets, and serve as the primary contact for sponsors and sites. With a deep understanding of clinical research processes, they balance structure with flexibility, always keeping the study’s big picture in sight.
- Their diplomatic mindset, creative problem-solving skills, and stress resilience are what allow them to thrive in dynamic environments—and to bring every project across the finish line.

Navigate challenges with confidence
From dynamic timelines to multi-stakeholder coordination and recruitment hurdles, our teams are built to anticipate, adapt, and act. Here’s how we address key challenges with structure and precision:
- Timeline Resilience: Our project teams maintain proactive planning buffers, use dynamic forecasting tools, and ensure constant alignment with all departments—keeping even complex, multi-country studies on track.
- Stakeholder Coordination: Juggle competing priorities across sponsors, CRO functions, sites, and vendors. We maintain clear communication channels, structured task distribution, and centralized documentation - ensuring transparency and reliability at every interface.
- Recruitment Support: Accelerate site activation and patient enrollment. We support feasibility processes, identify high-potential sites early, and maintain close communication with investigators - creating the operational foundation for successful recruitment strategies.

Latest Whitepaper
Our summarization of EUCROF's propositions on leveraging remote source data verification and reviews (rSDV/rSDR) in clinical trials. Gain insights and recommendations for seamless integration, ensuring data consistency and participant privacy while reducing site burden.
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