Clinical Data Associate II

📋 Description

• Supports data management from study start-up to post DB lock under supervision.
• Back-up to Lead DM to ensure timely, continuous task execution.
• Performs data entry for paper-CRF studies and data quality checks.
• Develops CRF specifications and coordinates stakeholder feedback.
• Conducts database build UAT and maintains QC docs.
• Reviews data per Data Management Plan; supports queries and reporting.

🎯 Requirements

• Bachelors and/or related experience.
• Around 2 years’ CDA experience in CRO/Pharma/Biotech.
• Proficiency in Word, Excel, PowerPoint, Outlook.
• Able to handle varied clinical research tasks.
• Excellent organizational and communication skills.
• Professional use of English; written and oral.

🎁 Benefits

• Equal Opportunity Employer.