Senior-level CRA expertise and a trusted network of clinical research professionals across Spain and Portugal.
Founded to deliver flexible, high-quality clinical trial support as a direct alternative to traditional resourcing models. Our team brings together Senior CRAs and Regulatory Specialists with over 10 years of hands-on experience across global CROs and sponsors.
Flexible monitoring, regulatory and site support across Spain & Portugal.
Scalable operational support for emerging clinical programs and lean study teams.
Support for investigator-initiated studies, academic research and foundation-sponsored projects.
Join our collaborative network for local monitoring and project-based support.
SSV, SIV, IMV, COV and remote monitoring. On-site and hybrid models.
Site feasibility, document collection, site activation and investigator communication.
CTIS submissions (Part I & II), Ethics Committees, Competent Authorities and document management.
eCRF review (Medidata Rave, Oracle, Inform), query management, data cleaning and database lock.
CRA · Lead CRA · Study Coordinator · CTA · Regulatory support · Local site management
Full remote monitoring capability with digital tools and structured oversight.
Site contract follow-up · Budget coordination · Hospital and foundation communication · Essential documents collection · Vendor coordination · Site activation support
We also support investigator-initiated studies (IIS), academic clinical research and foundation-sponsored projects, helping investigators navigate operational, regulatory and site-management requirements.
Operational Coverage
Madovi Research Solutions is strategically based in Galicia, providing highly cost-efficient access to major clinical research hospitals and trial-active regions across Northwest Spain and Northern Portugal.
For projects requiring broader national coverage, Madovi Research Solutions collaborates with an established network of experienced freelance CRAs located in key regions across Spain and Portugal.
This flexible operational model enables local CRA allocation whenever possible, helping reduce travel costs and improve operational efficiency for sponsors and CROs.
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Core operational hubs & CRA collaborator locations
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High-access clinical research regions

Flexible CRA coverage model optimized for regional efficiency and national scalability.
Our team brings over a decade of experience across global CROs and sponsors since 2014. Phases I, II, III and IV, interventional and observational studies across Spain and Portugal.
Phases I–IV clinical trials
CTIS regulatory submissions
Dual-country coverage: Spain & Portugal
A structurally different model compared to traditional hiring or large CRO engagement.
Engage project by project, scale as needed.
Clear pricing. No hidden HR or severance costs.
No juniors, no ramp-up time.
Reduced travel costs through site proximity.
From a single CRA to a full study team.
Freelance accountability with corporate-grade quality.
Experienced CRAs and clinical research professionals interested in flexible freelance collaboration across Spain and Portugal are welcome to contact us.
Collaborate With UsCRA support, regulatory expertise or flexible resourcing across Spain and Portugal — our team is ready.
Senior CRA expertise, regulatory submissions, and full study lifecycle support — engineered for sponsors and CROs who need flexible, accountable delivery from our team.