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Coding Specialist

Thermo Fisher Scientific
Thermo Fisher Scientific
1-2 years
₹4 LPA – ₹7 LPA (Estimated)
Remote
10 March 11, 2026
Job Description
Job Type: Full Time Remote 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

Job Title: Coding Specialist
Location: Remote, India
Company: Thermo Fisher Scientific
Employment Type: Full-time
Salary: ₹4 LPA – ₹7 LPA (Estimated)


Job Description

Thermo Fisher Scientific is hiring a Coding Specialist to join its Clinical Research Services team. In this role, you will ensure accurate and compliant coding of clinical and medical terminology according to established coding standards and study-specific Coding Plans. You will collaborate closely with Clinical Data Management (CDM) teams and study sites to identify data issues, resolve discrepancies, and deliver high-quality coding outputs aligned with regulatory guidelines, SOPs, and Good Clinical Practice (GCP).

This is a fully remote opportunity offering exposure to global clinical trials and collaboration with international teams supporting leading pharmaceutical and biotechnology companies.


Key Responsibilities

  • Perform medical terminology coding and review coding listings according to study Coding Plans and Data Validation Manuals (DVM).

  • Identify data discrepancies and coordinate with study teams and sites to resolve issues.

  • Ensure coding accuracy and compliance with departmental SOPs and regulatory standards.

  • Deliver coding outputs within quality expectations, project timelines, and budgets.

  • Provide guidance and support on coding activities to Clinical Data Management project teams.

  • Prepare and share regular project status reports with supervisors and clients.


Required Qualifications

  • Bachelor’s degree or equivalent relevant education.

  • 1 – 1.6 years of relevant experience in clinical data or medical coding.

  • Experience with RAVE / Veeva EDC systems.

  • Familiarity with WHODD and MEDDRA coding dictionaries.


Skills & Competencies

  • Strong understanding of clinical and medical terminology.

  • Knowledge of regulatory guidelines, SOPs, and clinical data standards.

  • Excellent attention to detail and analytical skills.

  • Good written and verbal communication in English.

  • Ability to work independently and in a team environment.

  • Strong organizational and problem-solving abilities.

  • Ability to maintain confidentiality of medical records and proprietary data.


Career Growth

This role provides exposure to global clinical research projects and opportunities to grow within the Clinical Data Management field. Potential career paths include:

  • Senior Clinical Data Manager

  • Clinical Data Team Lead

  • Clinical Data Management Project Manager

  • Data Standards / Programming roles


About the Company

Thermo Fisher Scientific is a global leader in scientific research services with more than 90,000 employees worldwide. The company supports pharmaceutical, biotechnology, and healthcare organizations in developing innovative therapies and advancing life-saving research.