Job Title: Clinical Data Coder I
Location: Thane, India (Hybrid Work Model)
Employment Type: Full-Time
Reference ID: R1525524
Industry: Clinical Data Management | Medical Coding | Clinical Research | CRO
IQVIA is hiring an experienced Clinical Data Coder I for its Clinical Data Management (CDM) team in Thane, India. This hybrid role is designed for healthcare and life sciences professionals with expertise 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 supports pharmaceutical and biotechnology companies by ensuring accurate, regulatory-compliant clinical data management across global trials.
The Clinical Data Coder I will independently manage coding activities for assigned clinical trial protocols. The role includes adverse event coding, medication coding, data validation, query management, and database lock support, ensuring high-quality deliverables aligned with sponsor and regulatory requirements.
The position may also involve supporting leadership functions such as Lead Coder or Data Operations Coordinator (DOC) for specific studies or coding-related tasks.
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 comprehensive data review and ensure coding accuracy and consistency.
Raise, track, and resolve data clarification queries.
Perform Serious Adverse Event (SAE) reconciliation in coordination with safety teams.
Manage coding activities throughout the clinical study lifecycle from study start-up to database lock.
Validate and test coding applications, reports, and related programming outputs.
Support testing of coding datasets, edit checks, and coding-related system validations.
Monitor and manage coding timelines in collaboration with Data Team Leads (DTL) and Managers.
Execute detailed quality control (QC) procedures for coding deliverables.
Ensure compliance with standard operating procedures (SOPs) and regulatory guidelines.
Support audit readiness and regulatory inspections for assigned studies.
Contribute to process improvements and implementation of new data management technologies.
Act as back-up to Lead Coder, Data Operations Coordinator (DOC), or Data Team Lead (DTL) when required.
Provide proactive coding-related solutions to the Data Management team.
Maintain effective communication with cross-functional teams, sponsors, and internal stakeholders.
Minimum 2 years of experience in Clinical Data Management or Medical Coding, or an equivalent combination of education and professional training.
Hands-on experience with MedDRA and WHO-DD coding.
Experience in SAE reconciliation and adverse event data review.
Understanding of the clinical data lifecycle and database lock processes.
Experience in a CRO or pharmaceutical clinical research setting 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 education with relevant clinical coding experience may be considered.
Strong knowledge of medical terminology, pharmacology, anatomy, and physiology.
In-depth understanding of medical coding dictionaries such as MedDRA and WHO-DD.
Familiarity with clinical database technologies and data management systems.
Excellent analytical ability and strong attention to detail.
Ability to work independently and resolve coding discrepancies efficiently.
Strong written and verbal communication skills in English.
Effective time management and organizational skills in a hybrid work environment.
Hybrid work model based in Thane, India.
Exposure to global, multi-center clinical trials.
Structured, compliance-driven clinical data management environment.
Opportunity to work with one of the world’s leading CRO organizations.
This role supports advancement in:
Advanced Clinical Data Management
Medical Coding Leadership
Data Operations Coordination
Regulatory & Safety Data Compliance
Potential career progression includes:
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 life sciences commercial intelligence. The company accelerates innovation in drug development through data-driven solutions and operational excellence.
If you have 2+ years of clinical data coding experience with MedDRA and WHO-DD expertise, this hybrid opportunity in Thane offers exposure to global clinical trials and advanced data management systems.
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