**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...