Informed Consent Codification Associate

Overview

Perform informed consent codification across multiple client instances, supporting clinical trial documentation at Labcorp.

What you'll do

• Perform informed consent codification across multiple client instances.
• Execute informed consent codification to completion correctly and meet delivery schedules.
• Apply strong troubleshooting and analytical skills to identify errors and determine 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.
• Knowledge of informed consent forms.
• Knowledge of global regulation and guidance documents in relation to informed consent information.
• Strong MS Office skills, particularly with Excel and Word.
• Strong communication and interpersonal skills.
• Problem solving and logic skills.
• Proven ability to plan, prioritize, and manage in a fast-paced environment with a high degree of initiative.
• Strong drive for process optimization and data integrity.
• Excellent attention to detail.
• Experience with 21 CFR Part 11 in a pharmaceutical, biotechnology, CRO, or related industry.

Nice to have

• Master's degree in science.
• 6 months of experience in programming languages and tools such as SQL and Python.

Details

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