CRENC consultants are researchers with a minimum of a Master degree and usually a PhD and at least five years of research experience.
Our consultants have the ability to perform any targeted research and provide a final report to our partners. They work quickly and efficiently, and deliver the services timely including when services are solicited at short notice. The work is always led by university professors and very experienced researchers.
When the skills required to perform a specific task are not available within the CRENC, our network always enables us to find experts in the specific areas.
CRENC research team supports pharmaceutical, biotechnology and medical industries in the form of research services outsourced on a contract basis. This include disease-registry and clinical-trial support for drugs and/or medical devices. Typically, this extends from conception and implementation to monitoring, and pharmacovigilance.
We offer technical assistance on the conduct of research projects from protocol development to publication. This include research question and methods refinement, CRF development, regulatory submissions, site feasibility of studies, data collection and cleaning, data management & bio-statistics, project management and clinical monitoring.
The CRENC team also supports foundations, research institutions, and universities, in addition to governmental organizations by offering our partners a satisfying solution for Data management services, from collection of data through to statistical and clinical reporting, that will not only prove cost efficient but we also commit to excellence. In short, we offer our partner the expertise to complete their clinical research from start to finish.