Job Title: Clinical Data Coder I
Location: Kochi, India (Hybrid Work Model)
Employment Type: Full-Time
Reference ID: R1525524
Industry: Clinical Data Management | Medical Coding | Clinical Research | CRO
IQVIA is hiring a detail-oriented Clinical Data Coder I to join its Clinical Data Management (CDM) team in Kochi, India. This hybrid role is ideal for life sciences and healthcare professionals with experience in medical coding, MedDRA, WHO Drug Dictionary (WHO-DD), SAE reconciliation, and clinical trial data review.
As a global leader in clinical research services and healthcare intelligence, IQVIA partners with pharmaceutical and biotechnology companies to accelerate drug development through high-quality clinical data management and regulatory-compliant coding practices.
The Clinical Data Coder I will provide comprehensive clinical coding and data management support across assigned study protocols. The role involves coding adverse events and medications, performing data validation, supporting database lock activities, and ensuring compliance with clinical data standards and SOPs.
The position may also include responsibilities as a Lead Coder or Data Operations Coordinator (DOC) for specific coding-related tasks or studies.
Independently serve as Clinical Data Coder for one or more clinical trial protocols.
Perform medical coding using:
MedDRA (Medical Dictionary for Regulatory Activities)
WHO Drug Dictionary (WHO-DD)
Conduct structured and ongoing data review to ensure coding accuracy and consistency.
Raise, track, and resolve data clarification queries.
Perform Serious Adverse Event (SAE) reconciliation activities.
Validate and test coding applications and related reports.
Support testing of coding datasets, edit checks, and related programming outputs.
Ensure data integrity from study start-up through database lock.
Monitor and manage coding deliverables within established project timelines.
Perform comprehensive quality control procedures for coding activities.
Ensure compliance with standard operating procedures (SOPs) and work instructions.
Support audit readiness and regulatory inspections for assigned studies.
Assist in implementation and adoption of new coding technologies and process enhancements.
Serve as back-up to Lead Coder, Data Operations Coordinator (DOC), or Data Team Lead (DTL) when required.
Provide coding-related insights and solutions to the Data Management team.
Maintain strong communication and working relationships with cross-functional teams and sponsors.
Minimum 2 years of experience in Clinical Data Management or Medical Coding, or an equivalent combination of education, training, and practical exposure.
Hands-on experience with MedDRA and WHO-DD coding.
Experience with SAE reconciliation and adverse event coding processes.
Understanding of the clinical trial data lifecycle, from study initiation through database lock.
Experience working in a CRO or pharmaceutical clinical research environment is preferred.
Degree in Pharmacy, Medicine, Dentistry, Nursing, Life Sciences, or related healthcare discipline.
Licensed Practical Nurse (LPN) licensure may be required where applicable.
Equivalent educational background with relevant clinical coding experience may be considered.
Strong knowledge of medical terminology, pharmacology, anatomy, and physiology.
In-depth understanding of medical dictionaries (MedDRA, WHO-DD).
Familiarity with clinical data management systems and database technologies.
High attention to detail and strong analytical skills.
Ability to work independently and resolve coding discrepancies proactively.
Excellent written and verbal communication skills in English.
Strong organizational and time management abilities in a hybrid work setup.
Hybrid work model based in Kochi, India.
Exposure to global, multi-center clinical trials.
Opportunity to contribute to regulatory-compliant clinical data processes within a leading CRO.
Collaborative and quality-focused clinical research environment.
This role offers professional development in:
Advanced Clinical Data Management (CDM)
Medical Coding & Safety Data Review
Data Operations Leadership
Regulatory Compliance & Clinical Data Standards
Potential career pathways include:
Senior Clinical Data Coder
Lead Coder
Data Operations Coordinator (DOC)
Data Team Lead (DTL)
IQVIA is a global provider of clinical research services, healthcare analytics, and commercial intelligence solutions for the life sciences industry. The organization supports pharmaceutical and biotech innovation through data-driven insights and high-quality clinical operations.
If you have 2+ years of clinical data coding experience with MedDRA and WHO-DD expertise, this hybrid opportunity in Kochi provides exposure to global clinical research programs and advanced data management systems.
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