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Clinical Data Coder 1 - India

2+ years
Not Disclosed
10 May 7, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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 1
Department: Clinical Data Management
Location: Kochi, Kerala, India
Job Type: Full-Time
Application End Date: 16 May 2025


Job Overview:

As a Clinical Data Coder 1, you will be responsible for coding-related tasks across the lifecycle of clinical studies, contributing to the accuracy and integrity of clinical data. You may serve as a Lead Coder or in other specialized roles such as a Data Operations Coordinator (DOC), handling coding activities independently or as part of a larger project team.


Key Responsibilities:

  • Serve independently as a Clinical Data Coder, Lead Coder, or DOC for one or more clinical protocols.

  • Manage the delivery of coding activities and/or stand-alone coding projects throughout the study lifecycle.

  • Validate and test coding applications, coding reports, datasets, and coding-related programming activities.

  • Conduct data review, write and resolve data clarifications, and perform serious adverse event (SAE) reconciliation activities.

  • Manage coding-related project timelines under the guidance of a DOC, Data Team Lead (DTL), or Manager.

  • Serve as a backup for Lead Coder, DOC, or DTL as required.

  • Perform comprehensive quality control procedures and assist in the implementation of new technologies.

  • Proactively bring coding and project-related solutions to the data management team.

  • Handle audit requirements for assigned studies, including stand-alone coding projects.

  • Comply with core operating procedures (COPs) and work instructions.

  • Foster and maintain effective communication and collaboration with the study team and manager.

  • Perform other study-related duties as assigned.


Qualifications:

  • Education:

    • Degree in Pharmacy, Dental, Medical, Nursing, Life Sciences, or a related field (or educational equivalent).

  • Experience:

    • Minimum of 2 years relevant experience in clinical data coding or a related role.

    • Equivalent combinations of education, training, and experience will be considered.

  • Skills & Competencies:

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

    • Proficiency with medical coding dictionaries (e.g., MedDRA, WHODD).

    • Solid understanding of data management processes from study start-up to database lock.

    • High attention to detail with the ability to work independently and solve problems proactively.

    • Familiarity with database technologies and data management tools.

    • Understanding and application of operating procedures and work instructions.

    • Excellent written and verbal communication skills in English.

    • Strong organizational and leadership capabilities.

    • Effective team collaboration with coworkers, managers, and clients.

  • Licensure:

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


About IQVIA:

IQVIA is a global leader in healthcare data science and clinical research, enabling smarter healthcare and life sciences decision-making. Our mission is to accelerate the development of innovative treatments and improve patient outcomes globally. Learn more: IQVIA Careers