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Data Team Lead

3-4 years
Not Disclosed
10 Oct. 28, 2025
Job Description
Job Type: Full Time Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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

Data Team Lead

Location: Kochi, India
Job ID: R1504546
Job Type: Full-Time | Hybrid
Additional Locations: Bengaluru, India | India


Job Overview

Lead end-to-end delivery of data management services for single or multi-service projects with minimal supervision. Ensure timely, high-quality, and cost-effective deliverables that meet customer expectations. Provide strong leadership and domain expertise to the Data Management (DM) team in project planning, execution, and closure while maintaining excellence in communication, quality, and compliance.


Key Responsibilities

  • Study Setup: Collect study setup requirements through discussions with stakeholders.

  • Device Integration: Support and oversee validation of new device integrations with minimal guidance.

  • Data Cleaning: Perform and oversee regular data cleaning activities to ensure accuracy and compliance with sponsor timelines.

  • Quality Oversight: Ensure all deliverables meet agreed quality standards and customer expectations.

  • Project Delivery: Ensure service quality and timelines are consistent with the contract or Scope of Work (SOW).

  • Training & Mentorship: Support onboarding and training of new joiners.

  • Meetings & Audits: Lead internal study meetings, sponsor audits, and participate in study kick-off and sponsor review meetings.

  • Project Management: Track and manage project progress, identify risks, and implement corrective actions when necessary.

  • Technology Implementation: Oversee implementation of new technologies or database updates with guidance.

  • Process Innovation: Collaborate with programming teams for process automation and efficiency improvements.

  • Compliance: Maintain compliance with required training, eSOPs, and regulatory guidelines.

  • Documentation: Review, develop, and maintain core operating procedures and work instructions.

  • Collaboration: Communicate effectively with line managers and cross-functional teams to ensure smooth coordination.

  • Other Duties: Perform additional responsibilities as directed by the line manager.


Qualifications

  • Education:
    Bachelor’s Degree in Health, Clinical, Biological, or Mathematical Sciences, or a related field (required).

  • Experience:

    • 3–4 years of direct Clinical Data Management (CDM) experience.

    • Minimum 1 year as a CDM Project Lead (preferred).

  • Skills:

    • Strong understanding of the drug development lifecycle and clinical research processes.

    • Advanced proficiency in Microsoft Excel, Word, and Outlook.

    • Excellent communication, leadership, and analytical abilities.

    • Fluent in spoken and written English.


About IQVIA

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We connect data, technology, and expertise to accelerate the development and commercialization of innovative medical treatments that improve patient outcomes and population health worldwide.

🌐 Learn more: https://jobs.iqvia.com


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