Clinical Data Associate II

Overview

The Clinical Data Associate II provides data management support across the clinical trial data management process from study start-up to post database lock, under direct supervision.

What you'll do

• Support the Lead DM to ensure timely task execution and continuity.
• Perform database development/testing and other data management activities as needed.
• Conduct quality control of data entry and assist with database builds and documentation.
• Develop CRF specifications from the clinical study protocol and coordinate stakeholder review.
• Review and query clinical trial data according to the Data Management Plan and perform line listings.
• Assist with SAE/AE reconciliation and medical coding for medical logic consistency.
• Liaise with third-party vendors (e.g., external data and EDC vendors) for data-related deliverables.

What you'll need

• 2 to 4 years’ experience.
• Proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook).
• Ability to handle a variety of clinical research tasks.
• Excellent organizational and communication skills.
• Professional use of English language (written and oral).
• Bachelor’s and/or a combination of related experience.

Nice to have

• Experience in a clinical, scientific, or healthcare discipline.

Details

• Location: Bangalore, Karnataka, India.
• May require some travel.