job_description.job_card.job_descriptionEntering and transcribing data from source documents to electronic systems (e.g., EDC, CRFs)Assisting with data verification and resolving discrepanciesPreparing for internal and external audits with clinical operations, quality, and regulatory teamsMaintaining accurate study tracking and timelinesCompleting required trainings and securing system accessCollaborating with Clinical Operations, Quality, Regulatory, CROs, Sponsors, and study staffEnsuring compliance with FDA regulations, ICH-GCP, SOPs, protocols, and company policies