- Noida, Uttar Pradesh, India
Responsible for medical coding services for clinical trials, ensuring accurate and timely deliverables.
Responsibilities
- Codes medical terms, adverse events, and concomitant medications using MedDRA and WHODrug across multiple clinical trials.
- Leads resolution of complex coding issues and discrepancies.
- Performs encoder user acceptance testing.
- Authors relevant sections of the data management plan (DMP).
- Ensures compliance with regulatory requirements for clinical trial coding (e.g., FDA, EMA).
Requirements
- Bachelor’s degree in a relevant medical field or equivalent work experience
- Nice to have: 2+ years of professional experience in medical coding in the clinical trials data space
- Nice to have: Familiarity with 21 CFR Part 11 or experience in a regulated environment