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Clinical Data Specialist

3+ years
₹8–12 LPA
10 Aug. 5, 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
Work Mode: Hybrid
Employment Type: Full-Time
Requisition ID: R1477949

Job Description:
IQVIA is hiring a Clinical Data Specialist to provide expert-level support to the eCOA (electronic Clinical Outcome Assessment) Data Management team. This role involves full-cycle clinical data management tasks, project oversight, and cross-functional collaboration to ensure high-quality data delivery in clinical trials.

Key Responsibilities:

  • Serve as Data Operations Coordinator (DOC) across multiple global clinical trials or lead specific data management tasks.

  • Act as a back-up for the Data Operations Coordinator or Data Team Lead as required.

  • Manage specific eCOA or clinical data management tasks independently.

  • Oversee entire data management process lifecycle, including timelines, resource planning, issue resolution, and out-of-scope identification.

  • Perform comprehensive quality control procedures and suggest process improvements.

  • Support implementation of new technologies and adhere to standard operating procedures (SOPs).

  • Build and maintain strong communication channels within the eCOA DM team and across project teams.

Required Qualifications & Experience:

  • Education: Bachelor's degree in Clinical, Biological, or Mathematical Sciences, or a nursing qualification.

  • Experience: Minimum 3 years in clinical trials, specifically in data management or related roles.

  • Strong understanding of data management processes, medical terminology, pharmacology, anatomy, and physiology.

  • Proven experience in managing large Phase I or medium-sized Phase III studies through the full data lifecycle.

  • Excellent organizational, communication, and analytical skills.

  • SAS knowledge is a plus but not mandatory.

  • Ability to work both independently and collaboratively with teams and clients.

About IQVIA:
IQVIA is a global leader in clinical research, healthcare analytics, and technology solutions for the life sciences industry. Our mission is to accelerate the development and commercialization of innovative treatments that enhance patient outcomes worldwide.

Estimated Salary: ₹8–12 LPA (based on role, experience, and industry standards)

Apply Now at IQVIA Careers