Informed Consent Codification Associate

Overview

Informed Consent Codification Associate I role performing informed consent codification across multiple client instances at Labcorp's Brigade Twin Tower office in Bangalore, India.

What you'll do

• Perform informed consent codification across multiple client instances.
• Execute informed consent codification to completion correctly and meet delivery schedules.
• Use strong troubleshooting and analytical skills to identify errors and resolution steps.
• Triage unacceptable errors for resolution.
• Maintain and utilize a strong knowledge of SOPs and validation work procedures/standards in relation to the System Development Life Cycle.

What you'll need

• Bachelor's degree in science.
• 6 months of experience in writing, reviewing, or reading informed consent for clinical trials.

Nice to have

• Master's degree in science.
• 6 months of experience in programming languages and tools such as SQL and Python.
• Experience with 21 CFR Part 11 in a pharmaceutical, biotechnology, CRO, or related industry.

Details

• Location: Brigade Twin Tower, Bangalore, India.
• Work schedule: Monday to Friday, rotating shift.