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.