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Clinical Data Management

Iqvia
IQVIA
3-4 years
Not Disclosed
10 Jan. 22, 2026
Job Description
Job Type: Full Time Remote 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

Job Title: Clinical Data Management – Data Team Lead
Location: Bengaluru / Pune, India (Home-based / Full-time)
Employment Type: Full-time, Regular
Requisition ID: R1523107


About the Role

IQVIA is seeking a Clinical Data Management (CDM) professional to lead end-to-end delivery of data management services for single- and multi-service clinical trials. As a Data Team Lead (DTL), you will provide expert oversight of clinical data management activities, ensuring quality, timeliness, and compliance with sponsor expectations. This role involves project leadership, financial management, process oversight, and team mentoring.


Key Responsibilities

  • Lead study setup activities, gathering requirements and aligning with stakeholders.

  • Oversee and validate new device integrations and database revisions.

  • Conduct and supervise data cleaning activities to ensure accuracy, completeness, and timely delivery of high-quality datasets.

  • Ensure all deliverables meet contractual, regulatory, and sponsor-defined quality standards.

  • Lead and participate in internal study meetings, sponsor audits, study kick-off meetings, and other project-related discussions.

  • Track project progress, identify risks, and implement corrective actions to meet timelines and quality metrics.

  • Collaborate with programming teams to drive process innovation, automation, and efficiency.

  • Support training and mentoring of new team members.

  • Review, maintain, and provide expert input on core operating procedures, SOPs, and working instructions.

  • Maintain compliance with trainings, eSOPs, and internal guidelines.

  • Communicate effectively with line managers and cross-functional team members.


Qualifications

  • Bachelor’s Degree in Health, Clinical, Biological, Mathematical Sciences, or a related field.

  • 3–4 years of direct Clinical Data Management experience, including a minimum of 1 year as a CDM project lead.

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

  • Proficiency in Microsoft Office applications (Excel, Word, Outlook) and data management tools.

  • Fluent in English, both spoken and written, with strong communication skills.


About IQVIA

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence. We connect data, technology, and expertise to accelerate the development and commercialization of innovative therapies, improving patient outcomes and population health worldwide. Learn more at IQVIA Careers.