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Clinical Data Specialist

Iqvia
IQVIA
2-5 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

Location: Kochi, Kerala, India
Employment Type: Full-Time | Hybrid
Job ID: R1519993
Experience Required: 2–5 Years (Clinical Data Management)

Job Overview

We are hiring a Clinical Data Specialist to support global clinical research programs by delivering high-quality clinical data management (CDM) solutions. This role involves hands-on data review, database development, and coordination activities to ensure accurate, compliant, and timely clinical data delivery. The position also offers opportunities to take on task-based leadership responsibilities under the guidance of senior CDM leadership.

Key Responsibilities

  • Provide clinical data management support to ensure efficient, accurate, and regulatory-compliant data delivery.

  • Serve as a Data Operations Coordinator (DOC) for:

    • A single protocol with fewer than five operations staff (excluding Data Entry), or

    • Fifteen or more easy to moderately complex central laboratory studies.

  • Act in a leadership role for specific CDM tasks such as clinical data coding, database testing, or database design (non-programming-intensive technologies).

  • Support or act as backup to the DOC or Data Team Lead (DTL) when required.

  • Perform clinical data review and discrepancy management, including writing and resolving data clarifications.

  • Lead or support database audits, ensuring adherence to quality standards.

  • Develop, test, and maintain clinical databases and edit check specifications.

  • Conduct testing of database programming and system functionality.

  • Perform clinical data coding using standard medical dictionaries.

  • Ensure compliance with core operating procedures (SOPs) and working instructions.

  • Meet assigned project objectives while maintaining strong collaboration and communication with CDM team members and stakeholders.

Qualifications & Experience

  • Bachelor’s degree in Clinical Sciences, Biological Sciences, Mathematical Sciences, or a related discipline.

  • Equivalent combinations of education, training, and relevant experience will be considered.

  • 2–5 years of experience in Clinical Data Management within a CRO, pharmaceutical, or life sciences environment.

  • Working knowledge of medical terminology and clinical trial data processes.

  • Strong organizational, analytical, and problem-solving skills with exceptional attention to detail.

  • Excellent written and verbal communication skills.

  • Ability to work independently, demonstrate initiative, and manage priorities effectively.

  • Proven capability to build and maintain effective working relationships with colleagues, managers, and clients.

  • Proficiency in clinical data management systems and standard office tools.

Why Join This Role

  • Opportunity to work on global clinical trials across multiple therapeutic areas.

  • Hybrid work model supporting work-life balance and flexibility.

  • Exposure to end-to-end clinical data management processes.

  • Career growth opportunities within clinical research and data operations leadership tracks.

About IQVIA

IQVIA is a global leader in clinical research services, commercial insights, and healthcare intelligence. By creating intelligent connections across the healthcare ecosystem, IQVIA accelerates the development and commercialization of innovative medical treatments, improving patient outcomes worldwide.

Apply Now

Qualified candidates with clinical data management experience are encouraged to apply through thepharmadaily.com.


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