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Executive - Clinical Data Coder

Sun Pharma
3+ years
₹6–10 LPA
Gurgaon, Gurugram, India
15 July 7, 2026
Job Description
Job Type: Full Time, Hybrid, Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance

Executive – Clinical Data Coder

Company: Sun Pharmaceutical Industries Ltd
Location: Gurgaon – R&D
Department: Clinical Data Management
Employment Type: Full-Time

Experience: Minimum 3+ years of experience in Clinical Data Coding with hands-on knowledge of medical coding dictionaries, coding tools, clinical data review, and discrepancy management.
Salary Package: ₹6–10 LPA (Approx., based on current market standards; final compensation depends on candidate experience, technical expertise, and skills.)


Role Overview

The Executive – Clinical Data Coder is responsible for performing clinical data coding activities across assigned clinical studies while ensuring compliance with company procedures, ICH-GCP guidelines, and applicable regulatory requirements. The role involves medical coding, data review, discrepancy resolution, coding validation, and collaboration with global clinical data management teams.


Key Responsibilities

Clinical Data Coding Activities

  • Perform clinical data coding activities for assigned clinical trials and projects.

  • Execute medical coding using relevant coding dictionaries, including:

    • MedDRA (Medical Dictionary for Regulatory Activities)

    • WHO Drug Dictionary

    • Other applicable medical coding dictionaries

  • Perform coding review and ensure accuracy, consistency, and completeness of coded data.

  • Support dictionary version upgrades and perform impact analysis where applicable.


Coding Validation & Database Support

  • Validate and test coding setup and programming of coding reports.

  • Support testing of clinical databases, edit specifications, and coding-related programming activities.

  • Identify and resolve coding-related issues and discrepancies.

  • Ensure coding processes meet project requirements and quality standards.


Clinical Data Review & Quality Management

  • Perform clinical data review, including medical data review activities.

  • Identify, document, and resolve data inconsistencies and discrepancies.

  • Perform Serious Adverse Event (SAE) reconciliation activities as required.

  • Ensure accuracy and completeness of clinical trial data.


Compliance & Documentation

  • Work in compliance with:

    • Sun Pharmaceutical procedural documents

    • Standard Operating Procedures (SOPs)

    • ICH-GCP guidelines

    • Applicable local regulatory requirements

  • Maintain appropriate documentation for coding activities.

  • Ensure adherence to quality standards and project timelines.


Cross-Functional Collaboration

  • Develop and maintain effective working relationships with global Clinical Data Management teams.

  • Collaborate with Clinical Data Management Project Leads and Coding Leads.

  • Support Clinical Data Management Reviewer activities when trained and assigned.

  • Participate in continuous improvement initiatives for clinical data processes.


Educational Qualification

  • Bachelor's degree in:

    • Life Sciences

    • Nursing

    • Pharmacy

    • Computer Science

    • Healthcare-related discipline

  • Relevant clinical data coding experience may be considered.


Required Experience

  • Minimum 3 years of Clinical Data Coding experience.

  • Hands-on experience with clinical data coding tools and applications.

  • Experience working with medical coding dictionaries such as MedDRA and WHO Drug.

  • Experience in global clinical studies is preferred.

  • Experience leading or coordinating clinical data coding activities is an advantage.


Technical Skills

  • Strong knowledge of clinical trial processes and clinical data management.

  • Experience with medical coding tools and clinical databases.

  • Understanding of SAE reconciliation processes.

  • Knowledge of ICH-GCP guidelines and clinical data standards.

  • Ability to perform data review and discrepancy management.


Key Competencies

  • Strong attention to detail and data accuracy.

  • Excellent analytical and problem-solving skills.

  • Good understanding of clinical research terminology.

  • Strong organizational and time management abilities.

  • Effective communication and collaboration skills.

  • Ability to work independently and within global project teams.

  • Commitment to quality, compliance, and data integrity.