A wide-range of clinical operations, regulatory and quality services from product design to final report.
Consulting activities are well known in clinical operations but Excelya has dramatically changed the paradigm by investing massively in our people who are our main asset.
We have developed an internal culture which allows each of our consultants to:
This approach makes a major difference in the way our people really integrate with our clients’ teams and bring added value, creativity and dedication.
Excelya operate as a fully-flexible and customizable Contract Research Organisation (CRO), with a tripartite solution offering, allowing clients to opt for a SLA which is fully tailored to their needs and their budget.
Option 1) Choose from full scale service, where Excelya manage your entire clinical trial operations as part of our Full Service CRO offering. This is a fully integrated service, with all operations, set up and recruitment included in the service.
Option 2) Alternatively, clients can opt for a more hybrid way of working, by employing Excelya as a Functional Service Provider. This setup allows you to retain more control and influence over your clinical trial, as Excelya are not fully managing the trial, but more of a bolt-on to your existing team and procedures.
Option 3) Finally, should your operational needs be smaller yet still require Excelya’s expertise, Operation Consulting could be the ideal option for your organization. Consulting allows you to onboard individuals or even a small team to help meet your short-term operational needs.
Clinical trials operational consulting is part of the Excelya DNA. Since our inception as a Contract Research Organization in France in 2014, we offered this service almost exclusively. We are glad to say that our business offering has evolved greatly based on client needs over the past 7 years, however clinical trials consulting remains a core pillar of our business model, largely due to the fact it is often the most practical and affordable option for many of our Biotech clients.
Based on our experience, the best way to guarantee that clinical trials will be delivered on time and on budget is by onboarding the most capable, specialized teams possible, with a work structure which allows us to streamline client needs in a way that is both efficient and cost effective. Consulting is uniquely effective in this regard, as sponsors can cater to their smaller-scale needs, and access Excelya’s experts on a flexible timeframe. This means that clients pay for the resources they need, when they need them, which allows them to be efficient and keep costs down without compromising on roadmaps, ambitions or deliverables.
Our consultants are selected either from our existing pool of more than 800 experts or sourced by our dedicated Talent Management team. Our bilingual and multinational teams can recruit globally, across multiple service and therapeutic areas. Our teams will compile a shortlist of candidates for client consideration, and clients can be as involved in the final stages of recruitment as they wish.
Excelya specialize in early phase consulting for clinical trials. Our services capabilities are extensive, covering data management to safety, project management, medical writing to regulatory affairs, and much more. Our diversity of skills allows us to add real value to our clients, with multi-skilled teams and specialists ready to go, with experience running trials of all sizes.