We are a small and flexible team of Clinical Project Managers, Clinical Research Associates, Regulatory Submission specialists, Site Contract Managers, Medical Consultants, Statisticians, PV Experts and Regulatory Affairs professionals who would bring you through your drug development journey. We mainly work on a freelance basis. In addition to that we partnered with a clinical database development partner who can create eCRFs, eQuestionnaires, ePatient Daries, ePROs and many other databases tailored to study needs.
Among our team are qualified physicians including specialists in Neurology and Cardiology.
has 14 years of clinical project management and monitoring experience, worked at small and global CROs like Medpace and Covance with a highest achieved title of a Senior Associate Director. In her career Anna was responsible for study delivery from the initial protocol design up to the final TMF transfer with global trial management experience in 29 countries on five continents with the largest study taking place in 24 countries and involving 200 sites.
We have extensive experience in Rare disease, Oncology, Neurology and Cardiology medical devices.
While being a small team of extremely dedicated individuals, we are looking to expand our crew of experts. If you are passionate about clinical research and looking to make a big impact with your contribution being highly visible and appreciated, do get in touch!
We are also very interested in expanding our network of potential partners and collaborators. If you are offering a unique service or simply want to network, we would be very happy to chat with you.
AnRes Clinical is open to flexible employment including part-time work, so you can give your best at your job while enjoying the time with your loved ones and feeling in control of your workload.