Clinical Research Specialist
CurrentDevelop and maintain study protocols, informed consent forms, and regulatory documents in compliance with applicable regulations and guidelines.Recruit and screen potential study participants, ensuring eligibility criteria are met.Collect and analyze clinical data, maintaining accurate records throughout the study.Facilitate communication between study sites, investigators, and sponsor organizations.Monitor study progress and ensure compliance with Good Clinical Practice (GCP) standards.Prepare and submit study progress reports, adverse event reports, and other regulatory documents as required.Assist in the preparation and coordination of Institutional Review Board (IRB) submissions and approvals.