About us
C-Trials is an independent Clinical Research Consulting firm providing expert clinical
monitoring, clinical operations support, and professional training to Sponsors, CROs,
Biotech, Medical Device companies, and Research Sites worldwide.
With decades of clinical research experience, we deliver flexible, high-quality solutions
that support the successful execution of clinical trials while ensuring regulatory
compliance, operational excellence, and the highest standards of patient safety.
At C-Trials, we work as a trusted extension of your team, combining scientific
expertise, professionalism, and a commitment to quality to help accelerate clinical
development and strengthen research capabilities across every phase of a study.We are Europe & Americas network of freelances of Clinical Research
Associates (CRA´s) and Clinical Research Professional Team with large
experience monitoring and managing clinical trials in Spain and Americas. Our
organization structure is diverse in experience and study development phase I-
IV clinical protocols sharing the same commitment quality, offering the best
solutions to our clients in oncology and rare diseases
C-trials established capabilities allow small and large sponsors alike to execute
any clinical trial, in any therapeutic área and country as our client requires
mission
To support clinical research organizations worldwide by providing high-quality
monitoring, consulting, and education that contribute to the successful execution of
clinical trials and the development of clinical research professionals.
vision
To become a trusted global partner recognized for excellence in clinical trial
consulting, monitoring, and professional education.
our goal
Our goal is to become a trusted clinical research partner for small and mid-sized
pharmaceutical, biotechnology, and medical device companies by delivering flexible,
high-quality clinical monitoring, operational support, and professional training. We are
committed to helping our clients accelerate clinical development, maintain regulatory
compliance, and achieve successful study outcomes through expertise, collaboration,
and personalized service.
Objective
To provide flexible, high-quality clinical research consulting, monitoring, and training
services that support Sponsors, CROs, Biotech, Medical Device companies, and
Research Sites in conducting compliant, efficient, and successful clinical trials.
Scope
C-Trials supports clinical research projects worldwide, offering expertise across all
phases of clinical development. Our services include clinical monitoring, clinical
operations support, site management, regulatory compliance, and professional training,
tailored to meet the specific needs of each client and study.
Services
Clinical Operations
Site selection (feasibility)
Site Initiation Visits
Interim Monitoring Visits
Close out monitoring visits
Database Lock Assistance
CRA Line Management
Study files Maintenance (TMF)
Management
Investigators Meeting Organization
Vendors selection and management
Sites contract negotiations
Training
Clinical monitors mentoring
CRA training
CRA Line management
Principal Investigators Training
Clinical Research Coordinators Training (CRC)
Therapeutic area trainings
Trainings on demand
Site Staff
Good Clinical Practice Training
Study files Maintenance (ISF)
Site staff trainings
Storage room maintenance
Other services
Decentralize Clinical Studies
Patient Home Assistance (included Latin America)
Therapeutic areas
We are rare little size clinical research organization team working on demanding research therapeutic areas as.
Rare Diseases
Rare diseases (RDs) are a severe, chronic, degenerative and often life-threatening group of conditions affecting more than 30 million people in Europe.
Their impact is often underreported and ranges from psychological and physical symptoms seriously compromising quality of life.
Around 80% of rare diseases are of genetic origin and, of those, 70% already start in childhood.
C-trials is committed with patients and research solutions participating to execute key clinical studies which contribute to improve patients quality life future and treatment access of major sponsors are working around the world.
Oncology
20+ years of experience in oncology clinical trials phase I-IV, observational and compassionate protocols
Therapeutic monitoring experience in solid and liquid tumors
Infection Disease
We are able to manage clinical trials in the following infectious diseases:
Coronavirus
Hepatitis
HPV
Acute rhinitis
Bacterial infections
Fungal infections
Gynecological infections
HIV infections
Meningitis
Dengue
Yellow fever
Devices
Medical device clinical research is a rapidly monitoring field that require
applications and other clinical research services. Also C-trials is committed in quality service to support your devices protocols.
Artificial Intelligence (AI)
Artificial intelligence is revolutionizing clinical research, accelerating the development of treatments and enhancing precision in the analysis of complex data. Its ability to process large volumes of information allows for the dentification of hidden patterns and the optimization of clinical trials, reducing costs and time. Additionally, it facilitates the personalization of therapies,
tailoring them to individual patient characteristics. AI is transforming medicine into a more efficient and effective approach, with the potential to save millions of lives.
CRA Benefits
Non cost Networking registration
Fees according experience and FTE
Central support Europe and Americas
Professional Insurance Advisory
International professional exposure
Innovation fields
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