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 focus on identifying and recruiting the most suitable experts for clients’ projects, based on our powerful HR team and methods which enable us to offer them relevant profiles, sometimes within a few hours.
Whether our mission is organized on a platform or otherwise, our operational teams work closely with team managers, allowing us to keep on schedule without any delay in the projects we lead. Our exclusive organization based on our teams’ human value is also the best way of guaranteeing our missions’ superlative quality. Our enthusiastic, reliable and creative teams commit themselves to our clients’ long term success, operating with unparalleled flexibility and team spirit in partnership with our clients’ teams.
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.
Thanks to its extensive network of KOLs and partners on the major continents, Excelya was able to find an extremely rare expert profile for a major pharmaceutical laboratory in just a few days. The client had struggled to find the right level of expertise for many months, resulting in the project concerned falling significantly behind their schedule. Available immediately, the new recruit was able to make up some of the time lost.
We were very impressed by the effectiveness of the EXCELYA process because we were able meet the candidate the day after having received the profile.
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.
