IQVIA Hiring Clinical Data Coder (MedDRA & WHO Drug)
Are you seeking IQVIA Careers India or Clinical Data Coder Jobs in India? Global clinical research giant IQVIA is recruiting experienced professionals for the position of Clinical Data Coder 1 (Job ID: R1525524) to support global clinical databases.
This medical terminology coding role is open to candidates with 1 to 10 years of experience who possess a background in Pharmacy, Dentistry, Nursing, or general Life Sciences. Selected coders will execute coding assignments using MedDRA and WHO Drug dictionaries. To draft a resume showcasing your database validation or discrepancy resolution metrics, read our guidelines on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particular | Details |
|---|---|
| Company | IQVIA (IQVIA India Private Limited) |
| Position | Clinical Data Coder 1 |
| Job ID | R1525524 |
| Work Locations | Bengaluru, Mumbai, Kochi, Kolkata, Ahmedabad, Noida (Hybrid Mode) |
| Experience Required | 1–10 Years (2+ years relevant experience preferred) |
| Qualifications | B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc Life Sciences, Nursing, Dental, or related field |
| Application Deadline | 17 July 2026 |
| Expected Salary | ₹4,00,000 – ₹12,00,000 per annum (Estimated based on experience) |
💼 Key Responsibilities
- Medical Coding: Code Adverse Events (AEs), medical histories, and concomitant medications using MedDRA and WHO Drug dictionaries.
- Lead Coder Support: Manage study-specific coding timelines, resolving data queries and database clarifications.
- Validation Testing: Validate coding tools and test database edit checks, query scripts, and coding datasets.
- SAE Reconciliation: Support Serious Adverse Event (SAE) database reconciliation tasks to align trial records.
- Timelines Delivery: Coordinate coding deliverables for global mega-trials under the direction of Data Team Leads.
- Quality Audits: Fulfill study audit requirements and ensure compliance with trial SOPs and ICH-GCP rules.
To learn how clinical coding salaries compare to conventional pharmacovigilance drug safety associate and clinical trial assistant structures, read our report on Pharmacovigilance Salary: India vs USA.
🎓 Required Qualifications & Skills
- Education: Bachelor's or Master's degree in Pharmacy, Nursing, Dentistry, Medicine, or related Life Science educational equivalents.
- Medical Dictionaries: In-depth knowledge of coding dictionaries (MedDRA, WHO Drug Dictionary/WHODD).
- Medical Foundations: Strong understanding of medical terminology, pharmacology, anatomy, and human physiology.
- CDM Understanding: Good knowledge of Clinical Data Management steps from study startup to database lock.
- Communication: Good written and verbal English communication for cross-functional study team emails.
For pharmacy graduates exploring data coding careers compared to conventional quality control chemistry or retail dispensing paths, read our analysis on B.Pharm Careers after Graduation: India vs USA.
🎁 Why Join IQVIA?
- Work with a leading global provider of clinical trials, analytics, and healthcare technology.
- Supportive hybrid work model combining home office efficiency with office collaboration.
- Diverse exposure managing large-scale global trials and safety reconciliation tasks.
- Paid parental leave, wellness initiatives, and clear career path charts.
To review your basic knowledge of clinical registries, patient protocols, and GCP guidelines before your interviews, try our interactive Clinical Trial Assistant (CTA) Quiz.
💡 Clinical Coder vs Healthcare IT
Clinical Data Coders review medical descriptions, map symptoms to MedDRA terms, and reconcile SAE drug reports, whereas Healthcare IT professionals support software deployments. To explore these differences, read our comparison on Healthcare IT vs Clinical Healthcare.
📝 Resume Tips for IQVIA Candidates
- Highlight Dictionary Coding: Explicitly mention MedDRA or WHODD updates/versions you have worked with (e.g., MedDRA v25).
- Specify Query Management: Detail your experience resolving coding queries or working on clinical database discrepancies.
- List EDC Experience: State the specific EDC systems (like Medidata RAVE, Oracle Clinical) you have used for coding reviews.
💬 IQVIA Clinical Data Coder Interview Questions
- Q1. What is the difference between MedDRA and WHO Drug dictionaries?
Answer Guidance: MedDRA (Medical Dictionary for Regulatory Activities) is used to code patient diagnoses, symptoms, medical history, and adverse events. WHO Drug Dictionary (WHODD) is used to code medicinal products, including active ingredients, chemical classes, and trade names. - Q2. How do you resolve a "Lower Level Term" (LLT) query when the investigator's term is vague?
Answer Guidance: I review the medical terminology and, if the term is too ambiguous to code safely, I issue a data clarification request (query) to the investigator to provide more specific clinical details. - Q3. Why is SAE reconciliation critical before database lock?
Answer Guidance: It ensures that safety databases (PV) and clinical trial databases (DM) match exactly regarding serious adverse events, ensuring accurate reporting to regulatory authorities.
🚀 How to Apply?
Interested and eligible candidates can submit their applications in two ways:
1. Email Application: Send your updated resume to:
Note: Please write "Clinical Data Coder Application" in the subject line of your email.
2. Online Application: Apply directly via IQVIA's Workday page:
Apply Online – IQVIA Workday Page❓ Frequently Asked Questions
Q. Which dictionaries are used for medical coding at IQVIA?
IQVIA clinical data coders mainly use MedDRA and the WHO Drug Dictionary (WHODD) for safety and medication coding.
Q. Are freshers eligible for this Clinical Data Coder opening?
This role requires at least 1 year (preferably 2+ years) of clinical coding or clinical data management experience.
Q. What is the application deadline?
Candidates must submit their applications (either via email or online workday form) before 17 July 2026.
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