Clinical Data Associate II

📋 Description \n \n Back-up to Lead DM; ensure continuity and timely tasks. \n Data entry for paper-CRF studies as needed. \n Quality control of data entry. \n Develop CRF specs from protocol; coordinate reviews. \n Assist in building clinical databases and UAT. \n Run patient and study status and metric reporting. \n \n 🎯 Requirements \n \n Bachelors and/or related experience. \n ~2 years’ CDA experience in CRO/Pharma/Biotech. \n MS Office proficiency: Word, Excel, PowerPoint, Outlook. \n Ability to handle a variety of clinical research tasks. \n Excellent organizational and communication skills. \n Professional English; written and oral. \n