Founded in 1997 by a Medical Doctors , Ergomed Plc is dedicated to the development of new drugs to save or improve lives. Operating with a global footprint in over 55 countries, Ergomed has the expertise to manage even the most challenging clinical trials.  Ergomed provides services to over 100 clients in a range of therapy areas but excels in the provision of services for  complex trials in Rare Diseases, Oncology and Neuroscience.

Duties and Responsibilities of the   Entry level/CRA

• Take ownership of assigned studies
• Carry out site selection and feasibility
• To act as the main point of communication with Investigator and the  team
• When requested to support preparation of regulatory / EC submissions
• Performing remote and on-site monitoring visits, site initiation and close out visits (remote and on-site)
• Office Based in Frankfurt/ Main

• College/University degree in Life Sciences or an equivalent combination of education, training & experience (minimum of a bachelor’s degree in a health or science related field)
• Native German (or at least C1)
• Full working proficiency in English
• Must maintain a valid driver’s license and the ability to drive to monitoring sites with the general ability to travel
• Proficient knowledge of Microsoft® Office
• Ability to plan, multitask and work in a dynamic team environment
• Communication, collaboration, and problem-solving skills
• Experience in a pharmaceutical or CRO setting preferred

We offer excellent chances to progress and develop. We work on a global basis on interesting projects within rare diseases, oncology, and neurology. This is an ideal position to develop a career in clinical drug development. It offers the chance to progress into clinical project management.