Clinical Research Coordinator
Current- Coordinate and manage multiple phase II-IV clinical researchstudies.- Ensure compliance with Good Clinical Practice (GCP) andapplicable regulations.- Maintain accurate and up-to-date study documentation.- Coordinate study visits, collect study data and answerqueries.- Communicate effectively with study sponsors, investigators,and study staff.- Schedules and participates in interim monitoring visits (IMVs),site management calls (SMCs), and close-out visits (COVs) forsource data verification (SDV).