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Coding Specialist

Thermo Fisher Scientific
Thermo Fisher Scientific
1-2 years
preferred by company
10 Jan. 9, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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 – Clinical Research (Remote, India)

Category: Clinical Research / Clinical Data Management
Job Type: Full-Time
Work Mode: Fully Remote
Location: India (Remote)
Job ID: R-01338263

Job Overview

Thermo Fisher Scientific is hiring a Coding Specialist to support global clinical research programs within its Functional Service Provider (FSP) model. This fully remote role is ideal for professionals with hands-on experience in medical and clinical coding who are passionate about data quality, regulatory compliance, and delivering inspection-ready clinical trial data.

As part of the Clinical Research Services team supporting the PPD® clinical research portfolio, you will contribute to high-impact global clinical trials across multiple therapeutic areas and phases.

Role Summary

The Coding Specialist is responsible for accurate and compliant coding of clinical and medical terminology using industry-standard dictionaries and study-specific coding plans. You will collaborate closely with Clinical Data Management (CDM) teams, study sites, and internal stakeholders to resolve data issues and ensure high-quality, analysis-ready datasets in alignment with SOPs, GCP, and Data Validation Manuals (DVMs).

Key Responsibilities

  • Perform medical and clinical terminology coding in accordance with study Coding Plans and DVMs

  • Review and maintain coding listings using standard dictionaries such as MedDRA and WHODrug

  • Identify coding discrepancies and collaborate with CDM teams and study sites for resolution

  • Ensure all coding activities meet quality, budget, and timeline expectations

  • Provide coding guidance and support to CDM project teams

  • Maintain accurate documentation and ensure inspection readiness

  • Generate and deliver regular project status reports for internal teams and clients

  • Adhere to global SOPs, regulatory guidelines, and client requirements

Required Education & Experience

  • Bachelor’s degree or equivalent qualification in life sciences, pharmacy, or a related field

  • Minimum 1 to 2 years of relevant experience in clinical data coding or clinical data management

  • Hands-on experience with EDC systems such as RAVE or Veeva EDC

  • Practical working knowledge of MedDRA and WHODrug (WHODD) coding dictionaries

  • Experience supporting global clinical trials is preferred

Key Skills & Competencies

  • Strong understanding of clinical and medical terminology

  • High attention to detail with excellent data quality focus

  • Knowledge of clinical trial protocols and Data Validation Manuals

  • Proficiency in interactive clinical data systems and MS Office tools

  • Strong written and verbal communication skills in English

  • Ability to work independently with minimal supervision in a remote environment

  • Strong organizational, analytical, and problem-solving skills

  • Proven ability to maintain confidentiality of medical and proprietary data

  • Flexible, adaptable, and collaborative team player with a strong customer focus

Career Growth & Development

This role supports a globally recognized biopharmaceutical sponsor known for innovation in specialty medicines and vaccines. As an FSP-dedicated employee, you will collaborate with international data science teams and contribute to complex, high-visibility clinical programs.

The FSP model offers structured learning paths, mentorship, and career progression opportunities. Depending on performance and business needs, you may advance into roles such as Senior Clinical Data Manager, Clinical Data Team Lead, CDM Project Manager, or transition into Data Standards or Programming functions.

Why Join Thermo Fisher Scientific

  • Work on global, multi-phase clinical trials across therapeutic areas

  • Gain end-to-end exposure to clinical data lifecycle activities

  • Build expertise in modern CDM tools, AI-enabled workflows, and global trial delivery

  • Collaborate with cross-functional teams across geographies

  • Be part of a mission-driven organization bringing life-changing therapies to patients worldwide

About Thermo Fisher Scientific

Thermo Fisher Scientific is the world leader in serving science, with annual revenue exceeding USD 44 billion. The company supports life sciences research, diagnostics, and pharmaceutical development through industry-leading brands including Thermo Scientific, PPD®, Patheon, and Applied Biosystems. With over 90,000 employees globally, Thermo Fisher Scientific is committed to making the world healthier, cleaner, and safer.

Equal Opportunity Employer: Thermo Fisher Scientific is an equal employment opportunity employer and values diversity and inclusion in the workplace.