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Clin Data Coder 2

4+ years
₹7–11 LPA
10 Aug. 13, 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

Clin Data Coder 2
Location: Kochi, India
Job Type: Full-time | Hybrid
Job ID: R1483628

Job Overview:
The Clin Data Coder 2 will deliver expert-level Clinical Data Management (CDM) coding services for global clinical trials, ensuring the accuracy, quality, and consistency of medical coding deliverables. This role involves working with standard medical dictionaries such as MedDRA, WHODD, and ICD9, managing coding activities throughout the study lifecycle, and serving as a Lead Coder, Coding Reviewer, or Subject Matter Expert (SME). The position requires collaboration with cross-functional teams, managing client relationships, and driving continuous process improvements in coding practices.

Key Responsibilities:

  • Independently serve as Clinical Data Coder, Lead Coder, and/or Coding Reviewer for one or more projects.

  • Act as account lead or main point of contact for standalone coding studies or accounts.

  • Manage delivery of coding activities through the full study lifecycle, ensuring compliance with timelines, budgets, and quality standards.

  • Validate and test coding applications, reports, and datasets; perform SAE reconciliation.

  • Conduct comprehensive data review, resolve coding-related queries, and ensure consistency in coding deliverables.

  • Implement process improvement initiatives and adopt best practices in coding operations.

  • Provide training, mentoring, and leadership to team members.

  • Maintain strong client relationships and manage coding-related negotiations.

  • Serve as back-up or act as Data Operations Coordinator (DOC) or Data Team Lead (DTL) when required.

Qualifications & Skills:

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

  • Experience: Minimum 4 years of relevant clinical trial experience in data management or medical coding.

  • Technical Expertise:

    • Proficient in medical dictionaries such as MedDRA, WHODD, ICD9.

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

    • Understanding of the drug development process and database technologies for data management and coding.

  • Soft Skills: Strong leadership, project management, communication, and client relationship management skills; ability to work independently and with cross-functional teams.

About IQVIA:
IQVIA is a global leader in clinical research, healthcare analytics, and commercialization services, leveraging advanced analytics and technology to drive innovation and improve patient outcomes.

Estimated Salary Range: ₹7–11 LPA (depending on experience and skills).