IQVIA Hiring – Clinical Data Coder 1 | Bangalore, Thane & Kochi
IQVIA, a global leader in clinical research and healthcare intelligence, is hiring for the role of Clinical Data Coder across Bangalore, Thane, and Kochi locations. This opportunity is suitable for professionals with 2 years of experience in clinical data coding who are looking to advance their career in clinical data management and coding operations.
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🏢 About the Company
IQVIA is a global leader in clinical research, healthcare data analytics, and technology solutions. The organization supports pharmaceutical and biotechnology companies across the entire drug development lifecycle. Working at IQVIA provides professionals exposure to global clinical trial standards, structured data management processes, and large‑scale multinational studies.
📊 Job Overview
- Position: Clinical Data coder 1
- Department: CDM
- Location: Bengaluru, Kochi, Thane
- Experience: 2+ Years
- Qualification: B.Pharm, M.pharm
- Job Type: Full-Time
- Last Date to apply: not provided
📋 Role & Responsibilities– Clinical Data coder 1 at Iqvia
- Work independently as a Clinical Data Coder, and when required, support activities as Lead Coder or Data Operations Coordinator (DOC) for one or more clinical study protocols.
- Manage delivery of medical coding activities and/or stand‑alone coding projects across the full study life cycle, with minimal supervision.
- Validate and test coding applications and coding reports.
- Test coding‑related datasets, edit checks, and other coding‑related programming activities as required.
- Perform comprehensive data review activities, including creation, resolution, and management of data clarifications related to coding.
- Manage coding project timelines in coordination with the DOC, Data Team Lead (DTL), or Manager, ensuring on‑time delivery.
- Perform Serious Adverse Event (SAE) reconciliation activities to maintain consistency between clinical and safety data.
- Conduct comprehensive quality control checks on coded data and deliverables.
- Support implementation of new tools, technologies, or process improvements within data management.
- Independently propose coding‑related and project‑level solutions to enhance data quality and operational efficiency within the DM team.
- Support audit and inspection requirements for assigned studies, including stand‑alone coding projects, ensuring inspection‑ready documentation.
🎓 Eligibility Criteria
- Candidates must meet the following requirements:
- Minimum 2 years of relevant experience in clinical data coding
- Background in Life Sciences, Pharmacy, Nursing, or related fields
- Proven experience in coding using MedDRA and WHO‑DD
- Strong foundation in medical and clinical terminology
- Ability to work independently on assigned coding tasks
🧠 Required Skills
The following skills are essential for this role:
- Strong knowledge of medical terminology, pharmacology, anatomy, and physiology
- In‑depth working knowledge of MedDRA and WHO‑DD (WHODD)
- Experience with clinical trial data coding workflows
- High attention to detail and data accuracy
- Analytical thinking and problem‑solving skills
- Good communication and documentation abilities
⭐ Job Role Insight
Clinical Data Coders play a critical role in ensuring that clinical trial data is standardized and reliable for analysis and regulatory submissions. Experienced coders contribute significantly to data quality by applying consistent coding practices and supporting downstream medical reviews. This role strengthens expertise in global coding standards and opens long‑term opportunities in clinical data management and safety operations.
🎯 Who Should Apply
This opportunity is ideal for:
- Professionals with 2+ years of clinical data coding experience
- Candidates experienced in MedDRA and WHO‑DD coding
- Individuals seeking growth in clinical data management
- Candidates experienced in regulated clinical research environments
💰 Salary Insight
- Compensation depends on experience level, location, and role scop
- Expected Salary: 4.5 to 7 LPA
💡 Preparation Tips
- Revise advanced MedDRA and WHO‑DD coding principles
- Strengthen knowledge of medical terminology and pharmacology
- Be prepared to discuss coding scenarios and consistency checks
- Highlight hands‑on project experience in your resume
🔗 Application Process
Interested candidates should apply only through the official company career website using the link provided below.
Important Disclaimer
This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official website before applying.
Similar Job : IQVIA Hiring – Clinical Research Coordinator | Bangalore
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❓FAQ-Clinical Data coder 1 at iqvia
1. Who can apply for the Clinical Data Coder role at IQVIA?
Candidates with qualifications in Pharmacy, Medical, Dental, Life Sciences, or related fields and around 2 years of experience in clinical data coding are eligible to apply.
2. What coding activities are involved in this role?
You will perform medical coding of adverse events and concomitant medications using industry‑standard dictionaries such as MedDRA and WHO‑DD, along with data review and clarification management.
3. Is experience with MedDRA and WHO‑DD mandatory?
Yes. Hands‑on experience with MedDRA and WHO‑DD is essential for accurate clinical data coding and regulatory‑compliant deliverables.
4. What is the level of independence expected in this role?
The role requires the ability to work independently on assigned coding activities and manage tasks with minimal supervision while collaborating with Leads and Managers as needed.
5. Will I be involved in end‑to‑end data management activities?
Yes. You will support coding activities across the entire data management lifecycle, from study start‑up through database lock, including SAE reconciliation.
