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Clinical Data Specialist

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

Job Summary:
IQVIA is seeking a Clinical Data Specialist in Bengaluru to lead eCOA data management activities across global clinical trials. The role involves coordinating clinical trial data operations, ensuring high-quality data deliverables, and supporting data reconciliation and monitoring tasks. Ideal for professionals with 3+ years of clinical data management experience, this role offers a hybrid work model and the opportunity to work on diverse clinical phases, including large-scale trials.


Key Responsibilities:

  • Act as Data Operations Coordinator (DOC) for multiple global clinical trials.

  • Lead or support specific eCOA data management tasks, including reconciliation and monitoring.

  • Oversee project timelines, data quality, and operational deliverables.

  • Identify and address out-of-scope tasks and escalate resource needs.

  • Implement and monitor quality control procedures across clinical data processes.

  • Support the Data Team Lead (DTL) as a backup when needed.

  • Communicate ideas for process improvements and assist in implementing new data management technologies.

  • Ensure adherence to standard operating procedures (SOPs) and project guidelines.

  • Collaborate with cross-functional teams to ensure timely and accurate data delivery.


Required Skills & Qualifications:

  • Bachelor’s degree in Clinical, Biological, or Mathematical Sciences (or equivalent healthcare/nursing qualification).

  • 3+ years of clinical data management experience, including Phase I–III clinical trials.

  • Knowledge of eCOA and clinical data processes across the study lifecycle.

  • Familiarity with SAS software (preferred but not mandatory).

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

  • Strong organizational, communication, and problem-solving skills.

  • Proven ability to manage project timelines, quality, and deliverables.

  • Detail-oriented with expertise in quality data review and reporting.


Perks & Benefits:

  • Opportunity to work on global clinical data management projects with industry leaders.

  • Exposure to cutting-edge eCOA data management technologies.

  • Professional development and training programs for career growth.

  • Hybrid work model for improved flexibility and work-life balance.


Company Description:

IQVIA is a global leader in clinical research, life sciences analytics, and healthcare data solutions. The company collaborates with pharmaceutical and healthcare organizations to accelerate medical innovations, enhance patient outcomes, and ensure regulatory compliance worldwide.


Work Mode: Hybrid – Bengaluru, India.


Call-to-Action:
Ready to advance your career in clinical data management? Apply now to join IQVIA as a Clinical Data Specialist and be part of global clinical trial innovations.