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Coding Specialist Ii

3-4 years
Not Disclosed
10 July 31, 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

 

Coding Specialist II – Clinical Data Coding (Bangalore)

Location: Bangalore, India
Category: Clinical
Work Mode: On-site or Hybrid (office/home-based setup)
Experience Required: 3–4 years (minimum 2 years in MedDRA/WHODrug coding)


Job Summary

Fortrea is hiring a Coding Specialist II to independently manage clinical medical data coding across global clinical trials. If you’re experienced with MedDRA, WHODrug, and dictionary tools like Medidata Coder, this role offers the opportunity to contribute to high-impact projects within one of the world’s leading Contract Research Organizations. This position is ideal for candidates with expertise in thesaurus management, GCP, and clinical trial operations.


Key Responsibilities

  • Execute medical coding tasks for global clinical projects using MedDRA and WHODrug

  • Collaborate with data reviewers and data management leads on study-specific coding conventions

  • Support setup and maintenance of coded clinical data and ensure regulatory compliance

  • Review and contribute to Data Management Plans and Coding Specifications

  • Perform dictionary verification and ensure coding quality across studies

  • Participate in SOP development and global process improvement initiatives

  • Liaise with cross-functional teams including programming, clinical operations, and safety

  • Support client satisfaction through on-time, accurate delivery of coded data

  • Maintain ongoing training in coding best practices and regulatory standards


Required Skills & Qualifications

  • Degree in Life Sciences, Pharmacy, Nursing, or allied health field

  • 3–4 years of experience in Clinical Data Management, including 2+ years in medical coding

  • Proficient in MedDRA and WHODrug coding systems

  • Experience using coding tools like Medidata Coder, Central Coding, etc.

  • In-depth knowledge of thesaurus management and clinical data management practices

  • Solid understanding of ICH-GCP and international regulatory standards

  • Strong verbal and written communication skills in English


Preferred Qualifications

  • MedDRA Certification

  • Experience with Fortrea SOPs and global coding conventions

  • Familiarity with client-specific medical dictionaries


Perks & Benefits

  • Global exposure to complex clinical research projects

  • Access to training and upskilling in advanced coding tools

  • Opportunity to work in a hybrid setup with flexibility

  • Career growth in pharmacovigilance and data coding

  • Collaborative work culture with cross-functional interaction


Company Description

Fortrea is a global Contract Research Organization (CRO) delivering innovative clinical development and technology solutions across more than 20 therapeutic areas. With operations in nearly 100 countries, Fortrea supports pharmaceutical, biotech, and medical device companies in bringing life-changing treatments to market faster.


Call-to-Action

If you're passionate about clinical data coding, thesaurus management, and want to make an impact in global clinical trials, apply now for the Coding Specialist II role at Fortrea in Bangalore. Start your journey toward meaningful work in a fast-paced healthcare environment.