Type permanent, office-based

Location: Western Austria

Are you an experienced CRA willing to progress in your career? Perhaps you have Degree in Pharamacy/Medicine or Science? Would you like to work within the field of medical devices? Sounds interesting? Well, our client is a leading global drug development company known for its excellence in the market place. As a result of rapid expansion a highly valued position CRA or Monitor has become available. By becoming a part of small but fast growing team you will have sound career perspectives and opportunities for further promotion.

Your principal responsibilities include but not limited to:

Provision of feasibility, site initiation, selection, monitoring and close out visits for clinical studies. You will conduct full cycle of CRA activities in compliance with international ICH/GCP standards and will extensively use SOP regulations. Being involved in liaison with investigators and sponsors you will be responsible for reporting on all protocol or ad hoc related issues to your project/line manager.

Your profile:

Degree in life science or/and medicine or extensive experience in clinical research. Demonstrated experience in monitoring of Clinical Studies is desired but not essential. Ability to work together with other departments and project teams in the region and across Europe. Strong PC skills with Microsoft Applications. Knowledge of ICH guidelines. Excellent presentation and communication skills will be required to provide liaison at all levels internally and externally. Fluency in English and German is essential. Ability to travel up to 50% is required. If for some reason this position is not of interest for you but you know someone suitable there is a bonus fee of EUR250 for every referred candidate that we successfully place.

In return our client will offer excellent career progression opportunities, competitive salary and remuneration package and an enviable working environment.