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Clinical Data Specialist

3+ years
₹8–12 LPA
10 Aug. 13, 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
Location: Bengaluru, India
Job Type: Full-time | Hybrid
Job ID: R1477949

Job Overview:
The Clinical Data Specialist will provide comprehensive data management expertise within eCOA (electronic Clinical Outcome Assessment) Data Management, ensuring high-quality deliverables that meet customer needs. The role involves supporting operational activities for eCOA Data Team Leads (DTL) or leading specific eCOA data management tasks such as data reconciliation, monitoring, and megatrial task leadership.

Key Responsibilities:

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

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

  • Provide domain-specific expertise in eCOA or Clinical Data Management tasks and technology.

  • Manage projects through the entire data management lifecycle, ensuring adherence to timelines, quality standards, and scope control.

  • Identify process improvements and assist in implementing new technologies.

  • Maintain compliance with standard operating procedures and working instructions.

  • Build strong communication channels with eCOA DM teams and project teams to ensure smooth operations.

Qualifications & Skills:

  • Education: Bachelor’s degree in clinical, biological, or mathematical sciences, nursing, or related field.

  • Experience: Minimum 3 years in clinical trials with a focus on data management; experience managing medium-to-large scale Phase I or Phase III studies.

  • Technical Skills: Working knowledge of SAS preferred but not required.

  • Knowledge Areas: Data management processes, medical terminology, pharmacology, anatomy, physiology, and the clinical drug development process.

  • Soft Skills: Strong organizational, detail orientation, problem-solving, and communication skills; ability to maintain effective working relationships with cross-functional teams.

About IQVIA:
IQVIA is a global leader in clinical research, healthcare data analytics, and commercialization services for the life sciences industry. The company leverages advanced analytics, technology solutions, and deep domain expertise to accelerate innovation and improve patient outcomes.

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