IQVIA Clinical Data Coding Opportunities Bangalore

IQVIA Hiring Clinical Data Coder 1 | BPharm, Life Sciences | Kochi, Bengaluru, Kolkata, Thane

IQVIA is hiring for the position of Clinical Data Coder 1 within its Clinical Data Management (CDM) division. This is a full-time hybrid role primarily based in Kochi, India, with additional opportunities available in Bengaluru, Kolkata, and Thane. The vacancy is suited for professionals with at least 2 years of relevant experience in clinical data coding, pharmacovigilance coding, or clinical data management. Candidates from pharmacy, nursing, dental, medical, and life sciences backgrounds are eligible to apply.

This opportunity is ideal for professionals aiming to build a stable and high-growth career in clinical data coding, medical coding, drug safety reconciliation, and global clinical trial data management within a leading multinational clinical research organization.

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Company Overview

entity[“organization”,”IQVIA”,”global healthcare analytics company”] is one of the world’s largest providers of clinical research services, healthcare analytics, and commercial insights for pharmaceutical, biotechnology, and medical device companies. Operating across more than 100 countries, IQVIA supports end-to-end drug development, from early clinical trials to post-marketing safety surveillance and commercialization strategies.

The company combines advanced data science, real-world evidence, and clinical trial technology to accelerate regulatory approvals and improve patient outcomes. IQVIA’s Clinical Data Management teams play a critical role in ensuring accurate, standardized, and regulatory-compliant data across global studies. Their work directly impacts database lock quality, regulatory submissions, and the safety evaluation of innovative therapies.

With strict compliance standards and a zero-tolerance approach to hiring fraud, IQVIA maintains a strong reputation for integrity and operational excellence in the healthcare and pharmaceutical industry.

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Job Role & Responsibilities

The Clinical Data Coder 1 will provide comprehensive coding and data management expertise to support sponsor requirements and internal quality standards. This role involves independent coding activities, medical dictionary management, SAE reconciliation, and database quality control throughout the full clinical study lifecycle.

Core Responsibilities

• Serve independently as a Clinical Data Coder, Lead Coder, or Data Operations Coordinator (DOC) for assigned protocols.
• Manage coding activities for standalone projects or full study lifecycles with minimal supervision.
• Validate and test coding applications and programming of coding reports.
• Test coding-related datasets, edit checks, and programming activities to ensure accuracy.
• Conduct detailed medical data review and resolve data clarification queries.
• Manage project timelines for coding deliverables in coordination with the Data Team Lead (DTL) or Manager.
• Perform Serious Adverse Event (SAE) reconciliation activities in collaboration with pharmacovigilance teams.
• Execute comprehensive quality control checks to maintain database integrity.
• Support implementation of new database technologies and system updates.
• Ensure compliance with SOPs, work instructions, and regulatory guidelines.
• Handle audit requirements and ensure inspection readiness for coding-related studies.
• Maintain professional communication with sponsors, managers, and cross-functional teams.

This role demands strong knowledge of medical terminology, pharmacology, anatomy, and physiology to ensure accurate coding using standardized medical dictionaries.

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Eligibility & Qualifications

Educational Background

Candidates must possess qualifications in pharmacy, medical sciences, nursing, dental sciences, or life sciences.

Eligible courses include:
B.Pharm, M.Pharm, Pharm.D, BDS (Dentistry), MBBS, BSc Nursing, GNM, LPN (Licensed Practical Nurse), BSc Life Sciences, MSc Life Sciences, BSc Biotechnology, MSc Biotechnology, BSc Microbiology, MSc Microbiology, BSc Biochemistry, MSc Biochemistry, Clinical Research, Allied Health Sciences, or equivalent educational background.

State Licensure as LPN is required where applicable.

Experience Requirements

• Minimum 2 years of relevant experience in clinical data coding, pharmacovigilance coding, or clinical data management.
• In-depth knowledge of medical dictionaries such as MedDRA and WHODD.
• Strong understanding of clinical trial data lifecycle from study start-up to database lock.
• Familiarity with database technologies and coding-related programming concepts.
• Excellent English communication skills, both written and verbal.
• Strong analytical thinking and attention to detail.
• Ability to resolve data discrepancies independently.

Candidates with prior exposure to SAE reconciliation, database validation, and global clinical trial coding projects will have an advantage.

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Location & Employment Details

• Primary Location: Kochi, India
• Additional Locations: Bengaluru, Kolkata, Thane
• Employment Type: Full-Time
• Work Model: Hybrid
• Job Requisition ID: R1525524

Application Process

Interested candidates can apply directly through the official IQVIA careers portal using the link below:

Apply Here: https://jobs.iqvia.com/en/jobs/R1525524-1

Applicants must ensure that all submitted credentials and experience details are accurate, as IQVIA follows strict compliance and background verification procedures.

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Frequently Asked Questions (FAQs)

1. Is prior coding experience mandatory?

Yes, candidates must have at least 2 years of relevant experience in clinical data coding or clinical data management.

2. Which medical dictionaries should candidates know?

Strong knowledge of MedDRA and WHODD is essential for accurate adverse event and medication coding.

3. Does the role involve pharmacovigilance activities?

Yes, SAE reconciliation and safety-related coding activities are part of the responsibilities.

4. Is this a remote role?

No, this is a hybrid role with office presence required in Kochi, Bengaluru, Kolkata, or Thane.

5. What is the career path after this role?

Professionals can move into Lead Coder, Data Team Lead, Clinical Data Manager, or global clinical operations leadership positions.

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Summary Table

Company	IQVIA
Vacancies	Clinical Data Coder 1
Required Education	B.Pharm, M.Pharm, Pharm.D, BDS, MBBS, BSc Nursing, LPN, BSc/MSc Life Sciences, Biotechnology, Microbiology, Biochemistry, Clinical Research
Experience	Minimum 2 years in clinical data coding or clinical data management