Clinical Research Associate, Single Sponsor dedicated in Poland

Job description

IQVIA is hiring Clinical Research Associates! Join IQVIA today and make an impact on patients’ outcome! Job Overview: Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Responsibilities: - Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation - Supporting the development of a subject recruitment plan - Establishing regular lines of communication plus administering protocol and related study training to assigned sites - Evaluating the quality and integrity of site practices – escalating quality issues as appropriate - Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution Qualifications: Minimum of a Bachelors Degree in scientific discipline or health care. Experience of 1 year in on-site monitoring clinical trials . Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmoniz...