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Discover A Career With Greater Purpose

Iqvia
IQVIA
2+ years
Not Disclosed
Bangalore, India
10 Feb. 12, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Data Coder I
Job ID: R1525524
Location: Bengaluru, India (Hybrid)
Job Type: Full-Time
Company: IQVIA

Experience Required
Minimum 2 years of relevant experience in clinical data management, medical coding, or related functions, or an equivalent combination of education, training, and experience.

Educational Qualification

  • Degree in Pharmacy, Medicine, Dentistry, Nursing, Life Sciences, or a related healthcare discipline, or equivalent educational qualification.

  • Licensed Practical Nurse (LPN) certification with state licensure may be required where applicable.

Role Overview
IQVIA is hiring a Clinical Data Coder I to support clinical data management and medical coding activities across clinical trials. The role involves coding clinical data using standardized medical dictionaries, managing data quality processes, and supporting study lifecycle activities from study start-up through database lock.

The position requires expertise in medical terminology, clinical trial data processes, and coding standards such as MedDRA and WHO Drug Dictionary. This role offers an opportunity to contribute to global clinical research programs and support the development of innovative healthcare solutions.

About IQVIA
IQVIA is a global leader in clinical research services, healthcare intelligence, and commercial insights for the life sciences and healthcare industries. The organization leverages advanced analytics, technology solutions, and scientific expertise to accelerate the development and commercialization of innovative medical treatments, improving patient outcomes and global population health.

Key Responsibilities

  • Perform clinical data coding and data management activities for assigned clinical trial protocols.

  • Serve independently as a Clinical Data Coder and may support responsibilities as Lead Coder or Data Operations Coordinator (DOC) when required.

  • Manage coding activities and deliverables across the full clinical study lifecycle with minimal supervision.

  • Validate and test coding applications, coding reports, and related programming outputs.

  • Review clinical data, generate data queries, and resolve data clarifications.

  • Perform Serious Adverse Event (SAE) reconciliation activities.

  • Support coding-related datasets, edit checks, and programming validation activities.

  • Manage coding timelines with guidance from Data Team Leads or project managers.

  • Perform quality control procedures to ensure data accuracy and regulatory compliance.

  • Support audit readiness and handle audit requirements for assigned studies.

  • Assist in implementing new technologies and process improvements within data management workflows.

  • Maintain compliance with standard operating procedures, work instructions, and regulatory guidelines.

  • Collaborate effectively with cross-functional teams, stakeholders, and study teams.

Required Skills and Competencies

  • Strong knowledge of medical terminology, pharmacology, anatomy, and physiology.

  • Expertise in medical coding dictionaries such as MedDRA and WHO Drug Dictionary (WHODD).

  • Understanding of clinical data management processes from study start-up to database lock.

  • Knowledge of database technologies and data management systems.

  • Strong analytical thinking and attention to detail.

  • Ability to work independently and resolve operational challenges.

  • Effective written and verbal communication skills in English.

  • Strong organizational and stakeholder management capabilities.

  • Ability to build and maintain professional relationships with teams and clients.

Work Environment and Career Growth

  • Hybrid work model with exposure to global clinical research projects.

  • Opportunity to contribute to large-scale clinical trials and healthcare innovation programs.

  • Continuous learning and professional development within clinical data management and coding domains.

  • Collaborative and performance-driven work environment.

Compliance and Integrity Statement
IQVIA maintains a strict zero-tolerance policy regarding candidate fraud. All information provided during the recruitment process must be accurate and complete. Any misrepresentation or false information may result in disqualification or termination of employment in accordance with applicable laws.

Equal Employment Opportunity
IQVIA is committed to providing equal employment opportunities and fostering an inclusive work environment for all employees and applicants.