Medical Coder – Principal (Fresher Friendly)
Location: Bangalore, Karnataka, India
Job Type: Full-time, Permanent
Experience Required: Fresher
About the Role
We are seeking a Medical Coder – Principal to join our Bangalore team. This role focuses on centralized medical coding, Serious Adverse Event (SAE) reconciliation, and supporting clinical trials with accurate, compliant coding. This position is ideal for freshers or candidates with academic/internship exposure in clinical research, pharmacovigilance, or medical coding.
As a Medical Coder, you will contribute to the integrity of clinical trial data by ensuring precise coding according to regulatory standards, MedDRA, and WHODrug dictionaries. You will collaborate with clinical, data management, and safety teams to maintain high-quality medical coding and SAE documentation.
Key Responsibilities
Perform accurate medical coding of clinical trial data using MedDRA and WHODrug dictionaries.
Assist in Serious Adverse Event (SAE) reconciliation across clinical databases and safety systems.
Document coding decisions, rationale, and ensure audit-ready records.
Support development and maintenance of Medical Coding Guidelines and SAE reconciliation processes.
Conduct reviews to ensure consistency and compliance with coding standards.
Collaborate with clinical, safety, and data management teams to resolve discrepancies in coding and safety data.
Assist in user acceptance testing (UAT) of coding tools and software as required.
Contribute to process improvements, coding tools, and data visualization for coding and SAE reconciliation.
Follow eClinical Solutions and industry quality standards, SOPs, and regulatory guidelines.
Participate in knowledge sharing, training, and mentoring within the coding team.
Candidate Profile
Education:
Bachelor’s degree in Health Sciences, Life Sciences, Pharmacy, or a related field.
Experience:
Fresher candidates are encouraged to apply. Internship or academic exposure in clinical trials, pharmacovigilance, or medical coding is advantageous.
Skills & Knowledge:
Basic understanding of ICH-GCP guidelines, 21 CFR Part 11, and clinical trial methodology.
Familiarity with MedDRA and WHODrug dictionaries.
Strong attention to detail, organizational skills, and ability to multitask.
Excellent verbal and written communication skills.
Ability to work independently as well as in a collaborative team environment.
Technical Skills:
Proficiency in Microsoft Office (Word, Excel, PowerPoint).
Exposure to electronic data capture (EDC) systems such as Medidata Rave Coder is a plus.
Why Join Us
Kickstart your career in medical coding and pharmacovigilance with exposure to global clinical trials.
Hands-on experience in regulatory-compliant medical coding processes and tools.
Work in a dynamic team environment with opportunities for mentorship and professional growth.
Contribute to high-quality clinical trial data that supports patient safety and regulatory submissions worldwide.
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