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Clinical Data Coder 1

Iqvia
IQVIA
2+ years
Not Disclosed
10 Feb. 11, 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

Job Title: Clinical Data Coder / Lead Coder – Clinical Data Management (CDM)
Company: IQVIA
Location: As per company requirements
Experience Required: Minimum 2 Years
Employment Type: Full-Time


Job Overview

IQVIA is seeking a skilled and detail-oriented Clinical Data Coder / Lead Coder to join its Clinical Data Management (CDM) team. This role is responsible for delivering high-quality, efficient data management and medical coding solutions to meet sponsor and organizational requirements across the full clinical study lifecycle.

The selected candidate will independently manage coding activities, support clinical data review processes, and may provide leadership in roles such as Lead Coder or Data Operations Coordinator (DOC). This position requires strong expertise in medical terminology, clinical databases, and global coding dictionaries, along with the ability to contribute to process optimization and quality compliance.

This opportunity is ideal for professionals looking to advance their career in clinical research, medical coding, pharmacovigilance, and clinical data management within a globally recognized organization.


Key Responsibilities

  • Serve independently as a Clinical Data Coder, Lead Coder, or Data Operations Coordinator (DOC) for one or more clinical trial protocols.

  • Manage end-to-end coding activities across the full study lifecycle, including standalone coding projects.

  • Validate and test coding applications, programming logic, coding reports, datasets, and coding-related edit checks.

  • Conduct comprehensive clinical data review, generate and resolve data queries, and ensure coding accuracy.

  • Oversee coding project timelines in collaboration with the DOC, Data Team Lead (DTL), or Manager.

  • Perform Serious Adverse Event (SAE) reconciliation activities in compliance with regulatory standards.

  • Execute quality control procedures to ensure data integrity and regulatory compliance.

  • Support the implementation of new technologies and process improvements within the Data Management team.

  • Contribute proactive solutions related to coding workflows and study deliverables.

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

  • Ensure adherence to Standard Operating Procedures (SOPs) and work instructions.

  • Act as backup for Lead Coder, DOC, or DTL when required.

  • Maintain effective communication and collaboration with cross-functional teams and stakeholders.


Required Qualifications

  • Degree in Pharmacy, Dentistry, Medicine, Nursing, Life Sciences, or a related field (or equivalent educational background).

  • Minimum 2 years of relevant experience in Clinical Data Management, Medical Coding, or related clinical research roles.

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

  • In-depth experience with global medical coding dictionaries such as MedDRA and WHODrug (WHODD).

  • Comprehensive understanding of the clinical data management lifecycle, from study start-up to database lock.

  • Familiarity with database technologies and systems used in clinical research data management.

  • Ability to work independently with strong analytical thinking and problem-solving skills.

  • Excellent attention to detail and commitment to data quality standards.

  • Strong written and verbal communication skills in English.

  • Proven organizational and leadership capabilities.

  • Ability to build effective working relationships with internal teams, managers, and external clients.

  • Licensed Practical Nurse (LPN) – State Licensure required, where applicable.


About IQVIA

IQVIA is a global leader in clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare sectors. The organization connects data, technology, and analytics to accelerate the development and commercialization of innovative medical treatments, ultimately improving patient outcomes and public health worldwide.


Integrity and Compliance Statement

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