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Coding Specialist (Senior Coding Specialist I)

Thermo Fisher Scientific
3+ years
Not Disclosed
Bangalore, India
2 May 21, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding

Coding Specialist (Senior Coding Specialist I)

Company: Thermo Fisher Scientific
Job Title: Coding Specialist (Senior Coding Specialist I)
Job ID: R-01352113
Location: Bengaluru, Karnataka
Job Category: Clinical Research / Clinical Data Management / Medical Coding
Employment Type: Full-time
Work Mode: Fully Remote
Work Schedule: Standard (Monday–Friday)


Job Summary

Thermo Fisher Scientific (PPD Clinical Research Services) is hiring a Senior Coding Specialist I to support clinical research studies by coding medical terminology, reviewing coding listings, resolving data discrepancies, mentoring coding teams, and ensuring compliance with GCP, SOPs, and study coding plans. This is an experienced clinical coding role within clinical data management.


Key Responsibilities

Medical Coding & Data Review

  • Code medical terminology according to:

    • Good Clinical Practice (GCP)

    • SOPs / WPDs

    • Data Validation Manuals (DVM)

    • Study-specific Coding Plans

  • Review coding listings for accuracy and completeness.

  • Identify data discrepancies and coordinate resolution with:

    • CDM project teams

    • Study sites

  • Ensure coding deliverables are:

    • Accurate

    • High quality

    • Within timelines

    • Within budget

Training & Leadership

  • Support coding training for Clinical Data Management staff.

  • Provide coding guidance to CDM project teams.

  • Mentor Coding Specialists and provide ongoing support.

Reporting & Coordination

  • Generate project-specific coding status reports for:

    • Supervisors

    • Clients

  • Support operational excellence across coding activities.

  • Maintain compliance with client expectations and regulatory standards.


Required Qualifications

  • Bachelor’s Degree or equivalent relevant academic/vocational qualification

Equivalent combination of education + relevant experience may also be accepted.


Required Experience

  • Minimum 3 years of relevant experience

  • Experience in:

    • Medical coding

    • Clinical data management

    • Clinical research operations