Do you have 2 years or more of monitoring experience? Maybe you are a CRA who wants to join a larger company? Are you striving for more responsibilities and career progression? 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 of CRA with Management responsibilities has become available.


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 manager. Results driven and
possessing leadership skills eventually you will be given Line and other Management
responsibilities.



Your profile:

Degree in medicine or pharmacy. Demonstrated experience in monitoring of Clinical Studies with at least 2 years within Clinical Research and ability to work together with other departments and project teams in the region and with the European offices. 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 Croatina is essential. Ability to travel up to 50% is required. If for some reason this position does not suit you but you know someone who might be interested there is a bonus fee of EUR250 for every candidate we successfully place