Clinical Data Associate II

📋 Description Support the Lead DM as back-up; ensure continuity and timely task completion. May perform data entry for paper-CRF studies as needed. May perform quality control of data entry. May develop CRF specifications from the protocol and coordinate reviews. Assist in building clinical databases. Conduct database build UAT and maintain QA documentation. 🎯 Requirements Bachelors and/or a combination of related experience. Around 2 years’ experience as a Clinical Data Associate for a CRO/Pharma/Biotech. Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook. Able to handle a variety of clinical research tasks. Excellent organizational and communication skills. Professional use of the English language; both written and oral.