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.
The role focuses on medical coding of clinical trial data, including adverse events and medications, using industry‑standard dictionaries and ensuring compliance with global data standards. Candidates will collaborate with data management and project teams to support accurate, high‑quality clinical trial data delivery.
This position offers strong exposure to global clinical studies, standardized coding practices, and long‑term career growth within IQVIA’s clinical data management organization.
Table of Contents
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
Key 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.
- Follow and comply with all core operating procedures (SOPs) and work instructions.
- Act as a backup resource for the Lead Coder, DOC, or DTL when required.
- Perform additional tasks and meet objectives assigned by the study team or Manager.
- Build and maintain effective working relationships with team members through clear communication and collaboration across functions.
Required Skills & Qualifications
- Qualification in Pharmacy, Dental, Medical, Life Sciences, or a related scientific field, or an equivalent educational background.
- Minimum 2 years of relevant experience in clinical data coding or an equivalent combination of education, training, and experience.
- Strong knowledge of medical terminology, pharmacology, anatomy, and physiology.
- In‑depth working knowledge of medical dictionaries used for coding, such as MedDRA and WHO‑DD (WHODD).
- Clear understanding of the Data Management lifecycle, from study start‑up through database lock.
- Good understanding of database technologies and systems related to data management and medical coding.
- Strong attention to detail with the ability to work independently, take initiative, and resolve coding‑related issues effectively.
- Good knowledge of operating procedures and work instructions, with the ability to apply them consistently in daily work.
- Excellent written and verbal communication skills in English.
- Strong organizational and leadership abilities.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
Why Join IQVIA?
- Benefit from continuous learning through training programs, new technologies, and opportunities to contribute solutions that improve coding and data quality.
- Collaborate with Data Team Leads, Managers, and cross‑functional teams in a professional environment that values communication, ownership, and teamwork.
- Your work directly supports data integrity, patient safety, and high‑quality clinical trial outcomes, contributing to the development of effective therapies globally.
How to Apply
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
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.
