Medical Coding Specialist Hiring Icon Plc | MedDRA, WhoDD

ICON Hiring Medical Coding Specialist for Clinical Data Management Teams

Global clinical research organization ICON plc has announced hiring for the role of Medical Coding Specialist I across multiple Indian locations including Bengaluru, Chennai, and Trivandrum. The opportunity is designed for life science and healthcare graduates interested in clinical trial data management and medical coding within global drug development programs.

For pharmacy and life science graduates looking to enter the clinical research industry, medical coding roles provide a strong entry into clinical data management and regulatory compliant data processing. Professionals working in this field help ensure that medical terms, adverse events, and drug information collected during clinical trials are accurately classified according to international coding standards.

With pharmaceutical companies increasingly relying on accurate clinical trial data for regulatory submissions, medical coding specialists play an essential role in maintaining the integrity and reliability of global clinical research databases.

Company Overview

ICON plc is a world-leading healthcare intelligence and clinical research organization that supports pharmaceutical, biotechnology, and medical device companies throughout the drug development lifecycle. The company offers services in clinical development, clinical data management, pharmacovigilance, regulatory strategy, and real-world evidence generation.

Operating across multiple countries, ICON collaborates with global pharmaceutical sponsors to accelerate clinical trials and support the approval of innovative medicines. The organization combines scientific expertise with advanced clinical technologies to manage complex clinical research programs.

ICON’s clinical data management and medical coding teams ensure that data generated during clinical trials is standardized, accurate, and compliant with regulatory guidelines required by health authorities such as the US FDA, EMA, and other global agencies.

Career Outlook for Safety Science Analysts and Medical Coding Professionals in 2026

The global clinical research industry continues to expand as pharmaceutical companies invest heavily in new therapies, vaccines, and precision medicines. By 2026, experts predict a growing demand for professionals specializing in clinical data management, safety science analytics, and medical coding.

Medical coding specialists play a critical role in organizing clinical trial data by translating medical terms, diagnoses, and adverse events into standardized coding dictionaries such as MedDRA and WHO Drug. These coded datasets allow statisticians, safety scientists, and regulatory teams to analyze clinical trial outcomes efficiently.

Professionals who begin careers in medical coding often progress into roles such as Clinical Data Manager, Drug Safety Associate, Pharmacovigilance Specialist, or Clinical Data Scientist. As clinical trials generate larger datasets, the need for skilled professionals capable of managing medical terminology and regulatory coding standards will continue to grow.

Job Role & Responsibilities

The Medical Coding Specialist will support clinical trial data quality by accurately coding medical terms and ensuring consistency across study datasets.

Key responsibilities include:

• Code medical terms, diagnoses, and procedures using standardized coding dictionaries such as MedDRA and WHO Drug
• Ensure consistent medical coding across multiple clinical trials and research programs
• Review clinical data entries to identify and resolve coding discrepancies
• Collaborate with clinical data managers, statisticians, and safety teams to maintain accurate datasets
• Provide guidance on coding standards and conventions used during clinical research
• Maintain updated knowledge of medical coding guidelines and regulatory requirements
• Contribute to process improvements that enhance the quality and efficiency of clinical trial data coding

These responsibilities help ensure that clinical trial datasets remain reliable and suitable for statistical analysis, regulatory submissions, and drug safety monitoring.

Eligibility / Qualifications

Candidates interested in this clinical research career opportunity should meet the following qualifications:

• Bachelor’s degree in Life Sciences, Pharmacy, Healthcare, or related discipline
• Understanding of medical coding systems such as MedDRA and WHO Drug
• Knowledge of clinical trial processes and clinical data management workflows
• Strong analytical thinking and attention to detail
• Good communication skills and ability to collaborate with cross-functional teams

Relevant education backgrounds may include: B.Pharm, M.Pharm, B.Sc Biotechnology, B.Sc Microbiology, B.Sc Biochemistry, B.Sc Life Sciences, M.Sc Clinical Research, M.Sc Biotechnology, PharmD.

Location & Salary

Location: Bengaluru, Chennai, and Trivandrum, India

Work Model: Office or hybrid work environment depending on project requirements.

Salary: Competitive clinical research industry salary based on experience and technical expertise. Leading CRO companies typically provide structured compensation packages, healthcare benefits, and professional development opportunities.

Benefits

ICON offers a range of employee benefits designed to support professional growth and work-life balance.

Benefits may include:

• Competitive salary and performance incentives
• Health insurance coverage for employees and families
• Retirement planning programs
• Global employee assistance support services
• Paid leave and flexible work arrangements
• Professional training and career development opportunities

These benefits support employees working in high-impact clinical research environments across global projects.

Application Process

Interested candidates can apply through the official ICON careers portal using the link below.

Apply here:
https://careers.iconplc.com/job/medical-coding-specialist-in-india-bangalore-jid-48901

Applicants should submit an updated resume highlighting their knowledge of clinical research, medical terminology, and medical coding systems.

Early applications are recommended as clinical data management roles in global CRO organizations often receive strong interest from qualified candidates.

Frequently Asked Questions

Who can apply for the ICON Medical Coding Specialist role?
Candidates with degrees in pharmacy, life sciences, healthcare, or related fields with knowledge of medical terminology and coding systems can apply.

Which coding dictionaries are used in clinical trials?
Clinical trials commonly use standardized medical dictionaries such as MedDRA and WHO Drug for coding medical terms and adverse events.

Is medical coding important for clinical research?
Yes. Accurate medical coding ensures that clinical trial data is standardized and suitable for statistical analysis, safety monitoring, and regulatory submissions.

What career growth opportunities exist in medical coding?
Professionals can advance into roles such as Clinical Data Manager, Pharmacovigilance Specialist, Drug Safety Associate, or Clinical Data Scientist.

Summary

Category	Details
Company	ICON plc
Vacancies	Medical Coding Specialist I
Required Education	B.Pharm, M.Pharm, B.Sc Biotechnology, B.Sc Microbiology, B.Sc Biochemistry, PharmD
Experience	Knowledge or experience in medical coding and clinical research
Location	Bengaluru, Chennai, Trivandrum
Department	Clinical Data Management

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