Medical Coder – Pharmacovigilance
Company: Veeda Lifesciences
Location: India (Location not specified)
Job Type: Full-Time
Experience: 2 – 4 Years
Qualification: Life Sciences / Pharmacy / Medical background preferred
Approx Salary: ₹4 LPA – ₹7 LPA
Job Overview
Veeda Lifesciences is hiring a Medical Coder – Pharmacovigilance responsible for managing medical coding activities in clinical studies. The role involves coding adverse events (AEs), medical conditions, and drug-related data using standard dictionaries such as MedDRA and ATC. The candidate will collaborate with clinical research, data management, and pharmacovigilance teams to ensure coding accuracy and compliance with study timelines and regulatory standards.
Key Responsibilities
1. Medical Coding Activities
Perform MedDRA and ATC coding for adverse events, medical conditions, and medication-related data.
Ensure coding activities are completed within agreed study timelines.
Maintain accuracy and consistency in coding terminology across clinical studies.
2. Study Data Management Support
Work closely with data managers, clinical scientists, programmers, and pharmacovigilance teams.
Raise queries in eCRF systems or other data platforms when coding clarification is required.
Review comments from sponsors or clinical science teams and update coded terms accordingly.
3. Documentation & Reporting
Prepare study coding reports and documentation for project tracking.
Maintain project management tools related to coding activities.
Track performance metrics and report backlog or potential challenges during study execution.
4. Training & Process Improvement
Prepare training materials for internal and external teams related to medical coding activities.
Provide on-the-job training for new team members.
Participate in periodic meetings within data management and statistics teams to promote best practices.
5. Compliance & Quality
Ensure compliance with company integrated management systems and international regulatory guidelines.
Maintain adherence to approved coding dictionaries and processes.
Support quality checks and coding review processes during clinical studies.
Required Skills
Technical Skills
MedDRA coding for adverse events and medical conditions
ATC coding for drug classification
Knowledge of clinical trial data management processes
Experience with Electronic Data Capture (EDC) systems such as Medidata Rave or Inform
Understanding of pharmacovigilance and clinical research workflows
Soft Skills
Strong attention to detail
Analytical and problem-solving abilities
Effective communication and collaboration skills
Ability to manage coding activities within strict timelines
Preferred Skills
Experience with clinical data management and database activities
Basic knowledge of programming languages or data management tools
Exposure to clinical database development, conduct, and close-out processes
Role Impact
The Medical Coder – Pharmacovigilance ensures accurate medical terminology coding and data consistency in clinical trials, enabling reliable safety data analysis and regulatory compliance for pharmaceutical research and drug development programs.
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