Job Title: Clinical Data Coder I
Location: Kolkata, India (Hybrid Work Model)
Employment Type: Full-Time
Reference ID: R1525524
Industry: Clinical Data Management | Medical Coding | Clinical Research | CRO
IQVIA is seeking a qualified Clinical Data Coder I to join its Clinical Data Management (CDM) team in Kolkata, India. This hybrid opportunity is ideal for healthcare and life sciences professionals with experience in clinical data coding, MedDRA, WHO Drug Dictionary (WHO-DD), SAE reconciliation, and clinical trial database management.
As a global leader in clinical research services and healthcare intelligence, IQVIA partners with pharmaceutical and biotechnology companies to ensure accurate, regulatory-compliant clinical data that supports global drug development and commercialization.
The Clinical Data Coder I will provide end-to-end coding and data management support across assigned clinical trial protocols. The role involves adverse event coding, medication coding, coding validation, data review, query resolution, and support through database lock activities.
The position may also include acting as a Lead Coder or Data Operations Coordinator (DOC) for specific tasks or studies, depending on project requirements.
Independently serve as Clinical Data Coder for one or more study protocols.
Perform coding using standardized medical dictionaries:
MedDRA (Medical Dictionary for Regulatory Activities)
WHO Drug Dictionary (WHO-DD)
Conduct comprehensive data review and ensure coding accuracy.
Raise and resolve data clarification queries.
Perform Serious Adverse Event (SAE) reconciliation activities in collaboration with safety teams.
Manage coding activities throughout the full 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 related system validations.
Monitor and manage coding deliverables in alignment with study timelines.
Execute detailed quality control (QC) procedures for coding deliverables.
Ensure adherence to standard operating procedures (SOPs) and work instructions.
Support audit readiness and regulatory inspection activities.
Contribute to implementation of new technologies and process improvements within the data management function.
Act as back-up to Lead Coder, Data Operations Coordinator (DOC), or Data Team Lead (DTL) when required.
Provide coding-related recommendations and solutions to the Data Management team.
Maintain effective communication with cross-functional teams, sponsors, and stakeholders.
Minimum 2 years of experience in Clinical Data Management or Medical Coding, or an equivalent combination of education and relevant training.
Hands-on experience with MedDRA and WHO-DD coding.
Experience in SAE reconciliation and adverse event data review.
Understanding of clinical trial data flow and database lock processes.
Experience in a CRO or pharmaceutical clinical research environment is preferred.
Degree in Pharmacy, Medicine, Dentistry, Nursing, Life Sciences, or a related healthcare field.
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 coding dictionaries (MedDRA, WHO-DD).
Familiarity with clinical data management systems and related database technologies.
Excellent analytical skills and attention to detail.
Ability to work independently and proactively resolve coding discrepancies.
Strong written and verbal communication skills in English.
Effective organizational and time management abilities in a hybrid work model.
Hybrid work model based in Kolkata, India.
Exposure to global, multi-center clinical research studies.
Collaborative, compliance-driven clinical data management environment.
Opportunity to work with a leading global CRO supporting innovative therapies.
This role provides advancement opportunities 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 leader in clinical research services, healthcare analytics, and life sciences commercial intelligence. The organization accelerates the development and commercialization of innovative therapies through data-driven insights and operational excellence.
If you have 2+ years of clinical data coding experience with expertise in MedDRA and WHO-DD, this hybrid opportunity in Kolkata offers exposure to global clinical trials and advanced clinical data systems.
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