Aurélie Weiss-Guimet, MSc, CEO of Expertrials
Our objective is to become an extension of your team by keeping a transparent and regular communication during each of your project steps.
ExperTrials is a clinical Contract Research Organisation (CRO) based in Lyon on a “human scale” founded in 2011 by Aurélie Weiss-Guimet and dedicated to startups in Biotech and Medtech with a 10-year experience with startups.
In the light of this extensive experience, we understand more than any other your need for flexibility and the ability to adapt with an optimal management of your budget. We know that your timelines are extremely tight in order to get the data needed to support the next round of funding and take the next step in the advancement of your clinical development programme.
Our expert team works closely with you to tailor the best solution for each project and to deliver clinical trials of the highest quality.
We provide complete solutions for clinical trials of any size, location and type, phase II-IV, drug or medical device and we have significant experience in both pre-approval and post-approval trials.
How does ExperTrials manage your budget and how you can save up to 40% compared to conventional CROs ?
With local expertise and focus on quality, ExperTrials ensures a high quality clinical trial management and on-time registration, while remaining within your budget.
In order to achieve this, ExperTrials has set up a new staffing organisational model with a flat hierarchy.
The leadership team is based at the headquarters in Lyon and our local teams consist of experienced Clinical Research Consultants across Europe, with additional partners in Israel, Canada, USA, Australia and Japan. In order to reduce the costs, ExperTrials does not have offices in each country and can therefore offer the most competitive prices compared to other CROs.
We offer you the complete solution – ExperTrials uses the most highly efficient tools in Clinical Research
Most highly efficient tools in Clinical Research are used at ExperTrials
eCRF : Rave Medidata is the most well-known EDC used by investigational sites
CTMS : Most efficient Clinical Trial Management System of Medidata will allow you to access your clinical study data anywhere and anytime
eTMF : Archiving of essential documents throughout your study in electronic format.
This helps you ensure you are inspection-ready at all times
goBalto Activate : study start-up tool to accelerate site activation
Docusign : Signature process of essential documentation throughout the trial is simplified, more efficient and reduce the costs by hundred of thousands euros
All data accessible anywhere, anytime and fully secured: You have access to your study data in real time. 0% paper, guaranteed 100% quality and GCP compliance.
We have the flexibility you need
Change is inevitable throughout clinical development. Working collaboratively and
strategically responding to change as it arises allows us to explore multiple
pathways to market.
We can tailor workflows and processes to consistently adapt to the dynamic
changes inherent in clinical research.
We have the flexibility to respond to changes through all phases of a project:
Industrial expertise to strategically guide evidence-based decisions
Flexible staffing to support every stage of a trial
We commit our expertise to your advantage
We have extensive experience from all aspects of the global drug development industry. We apply this diverse foundation of knowledge to strategically plan your project, identifying and mitigating potential risks to enable informed decision-making and project success.
Our Project Managers have an average of 10 years of experience and are well equipped to work alongside our client teams to develop strategy, maneuver challenges, and drive teams to meet and exceed study goals.
We proactively initiate transparent, collaborative communication
Our teams are flexible based on our flat hierarchy model, collaborative, transparent and we act as an extension of your team, relaying regular status updates as well as providing evidence-based recommendations to keep projects on track.
We proactively initiate transparent, collaborative communication throughout the trial lifecycle.
How do you benefit from transparent communications?
Team members are empowered to make decisions based on your study’s best interest
Proactive identification and communication of issues and solutions
Intensive study-specific training, cross-functional communication, and superior study team education ensure we always keep your end goal in mind
Engaging in a true partnership enhances operational success and your ability to get to market as efficiently as quickly as possible.