IQVIA Hiring Clinical Data Coder 1 Role: Pharma Jobs 2026

ByPharma Hiring Hub

IQVIA is hiring experienced professionals for the role of Clinical Data Coder, a great opportunity for candidates with around 2 years of hands‑on experience in clinical data coding and medical terminology. In this role, you will be responsible for coding clinical trial data using standardized medical dictionaries such as MedDRA and WHO‑DD, ensuring accuracy, consistency, and compliance with global data standards. This position is ideal for those looking to advance their career in clinical data management, coding operations, and biometrics within a leading global CRO.

Iqvia hiring Clinical Data coder 1 pharma jobs

Job Overview

  • Position: Clinical Data coder I
  • Department: Clinical research
  • Location: Banglore, Thane, kolkata, Kochi
  • Experience: 2 to 3 Years
  • Qualification: B.Pharm, M.Pharm
  • Job Type: Full-Time
  • Last date to apply: 04 March 2026

Key Responsibilities – Clinical Data Coder (IQVIA)

  • Independent Coding Support:
    Serve independently as a Clinical Data Coder, and when required, take on responsibilities as a Lead Coder or Data Operations Coordinator (DOC) across one or more clinical study protocols.
  • End‑to‑End Project Delivery:
    Manage and deliver coding activities and standalone coding projects throughout the entire study lifecycle, working with minimal supervision while ensuring quality and timelines.
  • Coding Application Testing:
    Validate and test coding applications, review coding reports, and assess programming outputs related to coding datasets, edit checks, or other coding‑related programming tasks.
  • Data Review & Clarifications:
    Perform comprehensive data management tasks, including data review, identification of discrepancies, and creation or resolution of data clarifications to maintain data accuracy.
  • Timeline & Project Coordination:
    Monitor and manage coding‑related timelines in collaboration with the DOC, Data Team Lead (DTL), or Manager, ensuring smooth study operations.
  • SAE Reconciliation:
    Execute Serious Adverse Event (SAE) reconciliation activities to ensure alignment between clinical and safety databases.
  • Backup Leadership Support:
    Act as a backup resource for the Lead Coder, DOC, or DTL, supporting study oversight whenever needed.
  • Quality Control & Technology Adoption:
    Perform thorough quality control checks, adhere to coding standards, and support the implementation of new tools, technology, and process improvements.
  • Proactive Problem Solving:
    Independently identify and provide coding‑related or study‑related solutions to the broader data management (DM) team.
  • Audit & Compliance:
    Manage coding documentation and deliverables required for audits, including standalone coding projects, ensuring readiness and compliance.
  • SOP & Process Adherence:
    Understand and follow all core operating procedures (SOPs) and relevant work instructions consistently.
  • Additional Responsibilities:
    Execute other tasks assigned by the study team or Manager and meet any additional study‑specific objectives.
  • Team Collaboration:
    Maintain strong communication and effective working relationships with cross‑functional team members, ensuring smooth project coordination.

Required Skills & Qualifications

  • A qualification in Pharmacy, Dental, Medical, Nursing, Life Sciences, or any related scientific field, or an equivalent educational background that meets clinical data coding requirements.
  • Minimum 2 years of relevant experience, or a suitable combination of education, training, and hands-on experience in clinical data coding or data management.
  • Strong understanding of medical terminology, pharmacology, anatomy, and physiology, essential for accurate interpretation and coding of clinical trial data.
  • In‑depth working knowledge of medical coding dictionaries such as MedDRA, WHO‑DD, and other standard classification systems used in clinical research.
  • Clear understanding of the clinical data management (CDM) lifecycle—from study start-up through data cleaning to database lock.
  • Excellent attention to detail with the ability to work independently, apply critical thinking, and proactively resolve coding or data discrepancies.
  • Good understanding of database technologies, EDC systems, and tools commonly used in data management and medical coding.
  • Familiarity with standard operating procedures (SOPs), work instructions, and the ability to apply them consistently in daily tasks.
  • Strong written and spoken English communication skills, along with organizational abilities and leadership qualities suitable for cross-functional collaboration.
  • Ability to build and maintain positive working relationships with team members, managers, and client team
  • LPN – Licensed Practical Nurse certification required when applicable, as per study or project needs.

Why Join IQVIA?

  • IQVIA is a global leader in clinical research, data science, AI‑driven healthcare solutions, and real‑world evidence. Being part of IQVIA gives you exposure to cutting‑edge tools, global clients, and high‑impact projects.
  • IQVIA provides continuous learning opportunities through training programs, mentorship, and access to industry‑leading technologies, helping you expand your knowledge in clinical data management, coding, biometrics, and regulatory sciences.
  • You get the chance to work with international teams, global sponsors, and multi‑country clinical studies, giving you hands‑on experience in large‑scale research operations.
  • IQVIA encourages innovation, problem‑solving, and process improvement. You’ll be part of a workplace that uses AI, machine learning, automation, and advanced clinical systems to streamline research.

How to Apply

Interested candidates should apply only through the official company career website using the link provided below.

Apply Here

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 IQVIA website before applying.

Similar Job from fortrea: Fortrea Hiring Freshers for Apprentice – Drug Safety (Pharmacovigilance)

FAQ – IQVIA Clinical Data Coder

1. What does a Clinical Data Coder do at IQVIA?

A Clinical Data Coder at IQVIA is responsible for coding medical terms using standardized dictionaries like MedDRA and WHO‑DD, resolving coding discrepancies, reviewing clinical data, performing SAE reconciliation, and supporting coding-related documentation for clinical trials.

2. How much experience is required for this role?

Candidates typically need 2 years of relevant experience in clinical data coding, clinical data management, or a similar role. Equivalent education and training may also be considered.

3. What educational qualification is needed?

Candidates should have a background in Pharmacy, Life Sciences, Nursing, Medical, Dental, or equivalent scientific fields. Some roles may also require LPN licensure, depending on project needs.

4. Do I need experience with MedDRA or WHO‑DD?

Yes. Strong knowledge and hands‑on experience with medical dictionaries such as MedDRA and WHO‑DD is essential for coding clinical terms accurately.

Similar Posts