This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Coding Specialist in India.
In this role, you will contribute to the accuracy, consistency, and quality of clinical trial data by performing advanced medical coding activities across global research projects. You will work within clinical data management teams to ensure that medical terms are correctly coded using standardized dictionaries such as MedDRA and WHODrug. The position plays a critical role in supporting clinical research operations by ensuring that coded data meets regulatory, quality, and client standards. You will collaborate closely with cross-functional stakeholders including clinical leads, statisticians, programmers, and safety teams. The environment is highly detail-oriented, global in scope, and focused on delivering high-quality data for life-saving therapies. This role is well suited for professionals who combine strong medical coding expertise with an interest in clinical research and data integrity.
Accountabilities:
- Perform independent medical coding activities for assigned global clinical research projects, ensuring accuracy and compliance with industry standards.
- Manage thesaurus and dictionary coding tasks using tools such as MedDRA and WHODrug to ensure consistent clinical data classification.
- Collaborate with clinical data management, safety, programming, and biostatistics teams to support end-to-end study setup, maintenance, and closeout activities.
- Review and support Data Management Plans and study-specific coding conventions to ensure alignment with project requirements.
- Identify and resolve coding-related issues, proposing improvements to enhance efficiency, quality, and consistency across projects.
- Support the development and implementation of SOPs, work instructions, and global coding best practices within the organization.
- Maintain technical expertise through continuous training and contribute to knowledge sharing within the team.
Requirements:
- 5–7 years of experience in clinical data coding within clinical trials or pharmaceutical/CRO environments.
- Strong knowledge of medical coding dictionaries such as MedDRA and WHODrug, along with experience using coding tools (e.g., Medidata Coder, Central Coding).
- Solid understanding of the clinical trial process, clinical data management, and regulatory requirements such as ICH-GCP guidelines.
- Familiarity with thesaurus management and global coding standards used in clinical research.
- Strong analytical skills with the ability to review medical literature and apply coding conventions accurately.
- Excellent communication and interpersonal skills to collaborate effectively across global, cross-functional teams.
- Bachelor’s degree in life sciences, pharmacy, nursing, or a related healthcare field (or equivalent professional experience).
- MedDRA certification and prior CRO or pharmaceutical industry experience are strong advantages.
Benefits:
- Competitive compensation aligned with experience and industry standards.
- Fully remote work arrangement based in India.
- Opportunity to contribute to global clinical research programs supporting life-saving therapies.
- Exposure to international cross-functional teams across clinical, safety, and data management domains.
- Continuous learning and professional development in clinical coding and regulatory standards.
- Structured, quality-driven work environment with clear processes and global best practices.
How Jobgether works:
We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.
We appreciate your interest and wish you the best!
Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time.
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