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Clinical Data Specialist

Iqvia
IQVIA
2-4 years
preferred by company
10 Jan. 13, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Job Title: Clinical Data Specialist – Bengaluru, India
Location: Bengaluru, Karnataka | Hybrid | Full-Time
Experience Required: 2–4 years in Clinical Data Management or related field

About IQVIA
IQVIA is a global leader in clinical research services, commercial insights, and healthcare intelligence, dedicated to advancing life sciences and improving patient outcomes worldwide. Our teams leverage innovative technology and data-driven solutions to accelerate the development of safe and effective medical therapies across diverse therapeutic areas.

Role Overview
IQVIA is seeking a Clinical Data Specialist to join our Bengaluru hub. The role provides essential data management expertise to the Clinical Data Management (CDM) team, ensuring high-quality data products and efficient study delivery. The position may include leadership responsibilities under the guidance of a Data Operations Coordinator (DOC), Data Team Lead (DTL), or Functional Manager.

Key Responsibilities

  • Act as a Data Operations Coordinator (DOC) for small to medium-scale protocols or support central laboratory studies.

  • Lead or support specific CDM tasks, including data coding, database design, data review, testing, and development of edit specifications.

  • Conduct data clarifications and resolve queries in compliance with study protocols and SOPs.

  • Participate in database audits, ensuring accuracy and adherence to quality standards.

  • Collaborate with internal teams and maintain effective communication with CDM team members, managers, and clients.

  • Ensure compliance with core operating procedures, regulatory guidelines, and study-specific requirements.

  • Take initiative in identifying and resolving data issues, demonstrating attention to detail and problem-solving capability.

Qualifications & Skills

  • Bachelor’s Degree in Clinical, Biological, or Mathematical Sciences, or related field.

  • Equivalent combination of education, training, and experience may be considered.

  • Exposure to medical terminology and clinical trial processes.

  • 2–4 years of experience in clinical data management, database testing, or related data operations.

  • Strong organizational, communication, leadership, and computer skills.

  • Ability to work independently, exercise initiative, and resolve problems efficiently.

  • Ability to build and maintain effective working relationships with cross-functional teams and stakeholders.

Why Join IQVIA?

  • Be part of a global team advancing life sciences and clinical research innovation.

  • Gain exposure to diverse therapeutic areas and cutting-edge clinical data management systems.

  • Opportunities for career growth, professional development, and leadership experience.

  • Work in a collaborative, hybrid environment that values expertise, innovation, and accountability.

Apply Now
Take your career to the next level by joining IQVIA’s Clinical Data Management team in Bengaluru. Submit your CV and cover letter online to be considered for this exciting opportunity.


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