Job Title: Clinical Data Coder I
Location: Bengaluru, India (Hybrid Work Model)
Employment Type: Full-Time
Reference ID: R1525524
Industry: Clinical Data Management | Medical Coding | Clinical Research | CRO
IQVIA is seeking a skilled Clinical Data Coder I to join its Clinical Data Management (CDM) team in Bengaluru, India. This hybrid opportunity is ideal for professionals with a background in life sciences, pharmacy, nursing, or medical disciplines who have experience in medical coding, clinical data review, and pharmacovigilance-related data processes.
As a global leader in clinical research services and healthcare intelligence, IQVIA supports pharmaceutical, biotechnology, and medical device companies in accelerating clinical development and improving patient outcomes.
The Clinical Data Coder I will provide comprehensive coding and data management expertise across clinical trials. The role involves medical coding using MedDRA and WHO Drug Dictionary (WHO-DD), SAE reconciliation, coding validation, and lifecycle data management support from study start-up through database lock.
This position may also involve acting as a Lead Coder or Data Operations Coordinator (DOC) for assigned protocols or coding-related tasks.
Independently serve as Clinical Data Coder for one or more clinical study protocols.
Perform medical coding using:
MedDRA (Medical Dictionary for Regulatory Activities)
WHO Drug Dictionary (WHO-DD)
Conduct data review, raise and resolve data queries, and ensure coding accuracy.
Perform Serious Adverse Event (SAE) reconciliation activities.
Validate and test coding applications, coding reports, and related programming outputs.
Support coding-related dataset testing and edit checks.
Manage coding activities across the full clinical study lifecycle with minimal supervision.
Monitor coding timelines and deliverables in coordination with Data Team Leads (DTL) or Managers.
Act as backup for Lead Coder, Data Operations Coordinator (DOC), or DTL when required.
Contribute coding solutions and process improvements to the Data Management team.
Perform comprehensive quality control (QC) procedures.
Ensure compliance with standard operating procedures (SOPs) and work instructions.
Support audit readiness and regulatory inspections for assigned studies.
Assist in implementation of new coding technologies and process enhancements.
Maintain strong working relationships with internal teams and sponsors.
Participate in study team meetings and provide coding-related insights.
Communicate effectively with cross-functional stakeholders.
Minimum 2 years of relevant experience in Clinical Data Management or Medical Coding, or an equivalent combination of education and training.
Hands-on experience in MedDRA and WHO-DD coding.
Exposure to SAE reconciliation and clinical database review processes.
Understanding of the clinical trial lifecycle from study start-up to database lock.
Degree in Pharmacy, Medicine, Dentistry, Nursing, Life Sciences, or a related healthcare discipline.
Licensed Practical Nurse (LPN) licensure may be required where applicable.
Equivalent educational background with relevant coding experience may be considered.
Strong knowledge of:
Medical terminology
Pharmacology
Anatomy and physiology
In-depth understanding of medical dictionaries used in clinical coding (MedDRA, WHO-DD).
Familiarity with database technologies related to clinical data management.
Ability to interpret and apply SOPs and regulatory guidelines.
Excellent attention to detail and analytical skills.
Strong written and verbal communication skills in English.
Ability to work independently and manage multiple priorities in a hybrid work environment.
Hybrid role based in Bengaluru, India.
Exposure to global, multi-center clinical trials.
Opportunity to work with one of the world’s leading CROs.
Collaborative and compliance-driven clinical research environment.
This role provides career advancement in:
Clinical Data Management (CDM)
Medical Coding & Safety Data Review
Data Operations Leadership
Pharmacovigilance & Regulatory Data Compliance
Potential progression paths include:
Senior Clinical Data Coder
Lead Coder
Data Operations Coordinator (DOC)
Data Team Lead (DTL)
IQVIA is a global provider of clinical research services, commercial insights, and healthcare intelligence for the life sciences industry. The organization supports innovative drug development and commercialization efforts worldwide through data-driven solutions and advanced analytics.
If you have 2+ years of clinical data coding experience with MedDRA and WHO-DD expertise, this hybrid opportunity in Bengaluru offers exposure to global clinical trials and advanced data management systems.
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