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Clinical Data Specialist

3+ years
Not Disclosed
10 July 24, 2025
Job Description
Job Type: Full Time Hybrid 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 – IQVIA, Bengaluru (Hybrid)

Job Summary:
IQVIA is hiring a skilled Clinical Data Specialist in Bengaluru to support global clinical trials with expertise in data management. The role involves delivering quality data solutions, managing eCOA data processes, and ensuring compliance with clinical research standards. Candidates with a strong background in clinical trials, data management, and knowledge of medical terminology will thrive in this hybrid role.


Key Responsibilities:

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

  • Support the Data Team Lead in operational eCOA Data Management activities.

  • Manage project timelines, data quality, and resource requirements.

  • Perform quality control procedures across the full data management life cycle.

  • Identify and address out-of-scope issues and propose project solutions.

  • Assist in developing and implementing new technologies for data management.

  • Maintain effective communication and collaboration with project teams.

  • Ensure adherence to standard operating procedures (SOPs) and working instructions.


Required Skills & Qualifications:

  • Bachelor’s degree in Clinical, Biological, or Mathematical Sciences (or Nursing qualification).

  • Minimum 3 years of experience in clinical data management and trials.

  • Knowledge of medical terminology, pharmacology, anatomy, and physiology.

  • Familiarity with SAS software (preferred).

  • Proven experience in managing data for large Phase I or Phase III clinical trials.

  • Strong organizational, communication, and detail-oriented data management skills.

  • In-depth understanding of the clinical drug development process.


Perks & Benefits:

  • Hybrid work environment in Bengaluru.

  • Opportunity to work on global clinical trials with industry-leading teams.

  • Professional growth and learning opportunities through advanced tools and technologies.

  • Exposure to cutting-edge eCOA data management practices.


Company Description:

IQVIA is a leading global provider of advanced clinical research services, commercial insights, and healthcare analytics for the life sciences industry. With a mission to improve patient outcomes and accelerate the development of innovative treatments, IQVIA leverages data, technology, and expertise to deliver exceptional solutions worldwide.


Work Mode: Hybrid – Bengaluru, India.


Call-to-Action:
If you’re ready to take the next step in your clinical data management career, apply now for the Clinical Data Specialist role at IQVIA and be part of a global leader driving healthcare transformation.