Clinical Research Coordinator
CurrentAccomplished Clinical Research Coordinator with background in managing clinical trials, ensuring patient safety, and maintaining compliance with GCP and ICH guidelines. Passionate about contributing to the advancement of medical knowledge and improving patient outcomes through efficient and ethical research practices. Experienced in collaborating with multidisciplinary teams, liaising with sponsors, and fostering relationships with study participants.• Coordinate and manage clinical trials in accordance with GCP and ICH guidelines• Collaborate with principal investigators, study sponsors, and multidisciplinary teams to ensure smooth study operations• Screen and recruit study participants, obtaining informed consent and maintaining strict confidentiality• Maintain accurate and up-to-date study documentation, including case report forms, patient records, and regulatory documents• Monitor and report adverse events, ensuring patient safety and proper documentation• Train and mentor junior staff members in clinical research best practices• Perform regular data quality checks and resolve data discrepancies