Clinical Data Coder

eClinical Solutions LLC

Bengaluru

On-site

INR 600,000 - 1,200,000

Full time

14 days+
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Job summary

eClinical Solutions LLC in Bengaluru seeks a Senior Medical Coder with 5-8 years of medical coding experience, preferably in the pharmaceutical industry. You will code clinical trial data using MedDRA terminology to ensure accurate reporting and regulatory compliance.

Review CRFs for completeness and accuracy, collaborate with project teams to resolve discrepancies, and ensure timely submission of high-quality coded datasets for trial reports.

Qualifications

  • 5-8 years of experience in medical coding, preferably in the pharmaceutical industry.
  • Strong knowledge of MedDRA terminology and guidelines for coding clinical trials.
  • Ability to work independently with minimal supervision while maintaining attention to detail and meeting deadlines.

Responsibilities

  • Code clinical trial data using MedDRA terminology to ensure accurate and consistent reporting.
  • Review case report forms (CRFs) for completeness, accuracy, and regulatory requirements.
  • Collaborate with project teams to resolve discrepancies or issues related to coding errors or missing data.
  • Ensure timely submission of high-quality coded datasets for inclusion in clinical trial reports.

Skills

MedDRA knowledge
Medical coding
Regulatory compliance
Attention to detail
Independent work

Job description

Roles and Responsibilities :
  • Code clinical trial data using MedDRA terminology to ensure accurate and consistent reporting.
  • Review case report forms (CRFs) for completeness, accuracy, and compliance with regulatory requirements.
  • Collaborate with project teams to resolve discrepancies or issues related to coding errors or missing data.
  • Ensure timely submission of high-quality coded datasets for inclusion in clinical trial reports.
Job Requirements :
  • 5-8 years of experience in medical coding, preferably in the pharmaceutical industry.
  • Strong knowledge of MedDRA terminology and guidelines for coding clinical trials.
  • Ability to work independently with minimal supervision while maintaining attention to detail and meeting deadlines.
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