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Clin Data Spec

1-3 years
Not Disclosed
10 June 25, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Clinical Data Specialist – Bengaluru, India (IQVIA)

Location: Bengaluru, India
Job Type: Full-Time
Work Mode: On-site / Hybrid (Not explicitly mentioned – likely office-based)
Experience Level: Entry-level to early-career


Job Summary

IQVIA is hiring a Clinical Data Specialist to support clinical data management activities for global pharmaceutical and healthcare trials. Based in Bengaluru, this role offers a unique opportunity to gain hands-on experience in central lab data management, database development, coding, and audit functions. Ideal for candidates with a life science background and strong attention to detail, this position supports global clinical development and regulatory efforts through accurate and high-quality data processing.


Key Responsibilities

  • Support data management activities across clinical protocols with guidance

  • Serve as Data Operations Coordinator (DOC) for small or moderately complex studies

  • Review clinical data and resolve data clarifications

  • Support audit teams and contribute to data quality checks

  • Participate in clinical data coding and documentation

  • Develop and test databases and edit specifications

  • Comply with CDM procedures and project-specific documentation standards

  • Maintain strong communication with cross-functional data teams


Required Skills & Qualifications

  • Bachelor’s degree in Clinical, Biological, Mathematical Sciences, or a related field

  • Familiarity with medical terminology and clinical data workflows

  • Strong organizational and problem-solving skills

  • Excellent communication and documentation skills

  • Attention to detail and ability to work with initiative

  • Comfortable with clinical data coding and database testing

  • Basic knowledge of clinical trials and pharmaceutical regulations preferred


Perks & Benefits

  • Opportunity to work on global clinical studies

  • Entry point into the clinical research industry with growth potential

  • Professional development and on-the-job mentoring

  • Work with cross-functional global teams

  • Exposure to IQVIA’s advanced healthcare data and analytics tools


Company Overview

IQVIA is a global leader in clinical research, real-world data, and healthcare intelligence. Supporting life sciences organizations in over 100 countries, IQVIA combines technology, analytics, and operational capabilities to accelerate the development and delivery of breakthrough medical treatments that improve patient outcomes.


Work Mode

On-site in Bengaluru, India (some hybrid flexibility may apply based on project needs)


Call to Action

Looking to kickstart your career in clinical data management? Join IQVIA as a Clinical Data Specialist and become a part of the global healthcare innovation movement.
Apply now to contribute to data-driven breakthroughs in clinical research.