Clinical Data Associate II

📋 Description Provide data management support from study start-up to database lock. Follow SOPs/WIs and regulatory directives across projects. Perform database development and testing, plus other data management activities. Back-up support for Lead DM to ensure continuity and timely task completion. May perform data entry for paper-CRF studies, as needed. May perform quality control of data entry. 🎯 Requirements Bachelors and/or a combination of related experience Around 2 years\' experience as a Clinical Data Associate in 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