Cononsulting and supporting companies in clinical trial management, building regulatory plans, clinical study planning, writing study documents, identifying suitable sites, and maintaining direct contact with physicians. The role also includes: Initiating and setting up clinical studies Clinical monitoring Building study teams Developing CRFs Writing protocols Leading trainings and instructional activities Working with CROs and vendors Providing comprehensive client support in this area Requirements: Bachelor’s degree in a relevant field – required At least 1 year of experience as a Clinical Research Coordinator or CRA – required Experience in pharma / biotech / medical device – required Experience in clinical trial management Experience in medical devices – a significant advantage Ability to work in a team, drive processes, and manage external service providers intensively Experience managing independent projects – an advantage Ability to support multiple projects simultaneously