Clinical Research Associate (m/f)

Our innovations have already increased the quality, safety and speed of drug development. Continued success has created excellent global opportunities for Clinical Research Associate (m/f) in our well established Zagreb office. As a Clinical Research Associate you will be responsible for performing and coordinating all aspects of clinical monitoring in compliance with ICH/GCP guidelines, local regulations and the company SOPs. You should thrive in multi-national project teams, be focused on delivering exemplary levels of customer service, as well as: - conduct feasibility and critically review feasibility assessments setting up the study centers, and provide regulatory submission support monitoring the trial throughout its duration, which involves visiting the study centers on a regular basis - verifying source documentation and data entered on to the CRFs writing visit reports; - filing and collating trial documentation and reports - maintain a close working relationship with the Clinical Operations Manager, Project Managers and the Pharma / Biotech sponsor

- medical education (MD), degree in pharmacy, university degree in life sciences - fluent knowledge of English and a driver's license (B category) - team oriented person, self-motivated with initiative - good time management skills - computer literacy - desire and ability to learn fast, work hard and travel a minimum of 50% of the time - minimum of 1 year experience as CRA