**Clinical Research Associate, Croatia**

-on site monitoring experience required-

**Your responsibilities will include:**

+ Performing site selection, initiation, monitoring and close-out visits
+ Supporting the development of a subject recruitment plan
+ Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
+ Collaborating with experts at study sites and with client representatives

**Qualifications:**

+ University degree in scientific discipline or health care
+ At least 1 year of on-site monitoring experience
+ Good knowledge of clinical research regulatory requirements
+ Very good computer skills including MS Office
+ Excellent command of Croatian...