Participate /nominate new sites for clinical studies; perform evaluation of site capability and make recommendation for inclusion in clinical trial. Assist in managing clinical study projects, ensuring on-time & on-budget performance. Ensure site activities in line with milestones (i.e. startup, recruitment, closeout, etc). Perform site-start-up activities (submissions to ethics committees, institution review board). Execute site initiation and training activities. Monitor (pre-study, initiation, routine, and close-out visits) investigator sites for Good Clinical Practice (GCP) compliance according to Abbott SOPs and relevant FDA, NMPA regulations. Resolve issues, questions, and requests for additional study supplies. Review and verify completed CRFs. Evaluate data and/or monitoring reports for protocol violations and serious protocol deviations, and proactively address violations/deviations