SSU Clinical Research Associate, Single Sponsor dedicated in Poland

Job description

IQVIA is hiring Study Start-up Clinical Research Associates! Join IQVIA today and make an impact on patients’ outcome! Job Overview: Perform monitoring, study start-up 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 - Responsible for Study Start-Up activities. - 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...