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Clin Data Specialist

0-2 years
Not Disclosed
10 Nov. 26, 2025
Job Description
Job Type: Full Time Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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

Location: India (Hybrid)
Employment Type: Full-Time
Job ID: R1483495
Company: IQVIA

Overview

IQVIA, a global leader in clinical research, healthcare analytics, and real-world evidence, is seeking a Clinical Data Specialist to support clinical data processes across a wide range of clinical studies. This role involves ensuring high-quality data review, supporting data management activities, and collaborating with cross-functional teams to drive clinical trial excellence. The ideal candidate will possess strong analytical abilities, attention to detail, and the capability to work independently in a fast-paced environment.

This position is available across multiple locations in India, including Bengaluru, with hybrid work flexibility.


Key Responsibilities

  • Perform clinical data review and validation activities according to project timelines and quality expectations.

  • Ensure accuracy, consistency, and completeness of clinical study data across assigned studies.

  • Apply knowledge of medical terminology, data management processes, and study protocols to support decision-making.

  • Identify, investigate, and resolve data queries and discrepancies.

  • Collaborate with cross-functional teams, including data managers, clinical teams, and project stakeholders.

  • Maintain detailed documentation related to data review activities, data quality checks, and issue tracking.

  • Support continuous improvement initiatives by recommending process enhancements.

  • Coordinate with study teams to ensure adherence to study timelines, data standards, and regulatory requirements.

  • Contribute to database development, edit check design, and user acceptance testing as applicable.

  • Uphold IQVIA’s data integrity standards and operational excellence culture.


Required Qualifications

  • Bachelor’s degree in Clinical Research, Biological Sciences, Mathematical Sciences, or a related discipline.

  • Equivalent education, training, or experience may be considered in lieu of a formal degree.


Experience Requirements

  • Prior exposure to medical terminology is required.

  • Experience in clinical data management, clinical research operations, or related functions is preferred.

  • Strong organizational skills with proven ability to handle multiple tasks.

  • Demonstrated experience working independently, solving problems, and managing priorities.

  • Ability to maintain effective working relationships with team members, managers, and external clients.

  • Proficiency in computer applications, data systems, and analytical tools.


Skills and Competencies

  • Strong written and verbal communication skills.

  • High attention to detail and quality-driven mindset.

  • Ability to work with initiative and minimal supervision.

  • Strong leadership potential and team collaboration abilities.

  • Ability to analyze issues and apply logical problem-solving approaches.


About IQVIA

IQVIA is a global leader in advancing healthcare through analytics, technology, and clinical research. The company partners with life sciences organizations worldwide to design and deliver innovative clinical solutions that accelerate the development of new therapies and improve patient outcomes.

Learn more at: https://jobs.iqvia.com