Catherine Ferrari

I started in clinical research through studies in the pharmaceutical industry. I then joined a medical device company. I trained in the new regulations and new standards. I fully invested myself in this activity, from the development of protocols and CRFs to the implementation of studies, monitoring, study reports, site closure, management and training, and adverse event monitoring. I then became a project manager and now I wish to work as a freelancer, preferably in medical devices. I mainly work on observational studies but can work on interventional studies. I have good interpersonal skills, which are important in this profession. I am available, rigorous, and serious in my work. I have dual expertise as a Clinical Research Associate and Pharmacovigilance Specialist.