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40151 Assoc Mgr, Clin Data Mgmt

Iqvia
IQVIA
5 years
Not Disclosed
Bengaluru, India
10 Feb. 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

Associate Manager – Clinical Data Management

Location: Bengaluru, India
Employment Type: Full-Time
Work Model: Hybrid
Industry: Clinical Research / Life Sciences

A global leader in clinical research and healthcare intelligence, IQVIA, is seeking an experienced Associate Manager – Clinical Data Management to lead and oversee a team of data management professionals. This leadership role is responsible for ensuring high-quality database delivery, operational efficiency, and compliance within clinical development programs.


Job Overview

The Associate Manager – Clinical Data Management will manage and mentor a team of clinical data professionals to deliver accurate, regulatory-compliant clinical databases aligned with sponsor requirements. The role involves strategic resource planning, performance oversight, proposal support, stakeholder engagement, and continuous process improvement within the clinical data lifecycle.

This position requires strong leadership capabilities, deep knowledge of data management systems, and a broad understanding of the clinical drug development process.


Key Responsibilities

  • Lead and manage a team of 4–8+ Data Management professionals

  • Plan and allocate resources across multiple clinical projects

  • Ensure optimal staff utilization and performance management

  • Review and provide expert guidance on database design, validation programming, and data deliverables

  • Oversee production of data management documentation and regulatory-compliant outputs

  • Ensure timely achievement of project milestones with high-quality standards

  • Participate in proposal development, scope discussions, and client presentations

  • Identify out-of-scope work and support cost estimation processes

  • Drive implementation of new technologies and process improvements

  • Ensure compliance with SOPs, regulatory requirements, and project scope

  • Mentor and develop team members to enhance technical expertise

  • Manage HR responsibilities including performance evaluation, recruitment participation, and employee development


Experience Level: Mid-Senior Level

Experience Required:

  • Minimum 5 years of relevant experience in Clinical Data Management

  • Prior team leadership or supervisory experience preferred

  • Advanced knowledge of clinical data management systems and processes

  • Strong understanding of clinical trial lifecycle and drug development processes

  • Experience interacting with sponsors and managing client-facing deliverables


Educational Qualification

  • Bachelor’s Degree in Clinical, Biological, Mathematical Sciences, Nursing, or related field

  • Equivalent combination of education and relevant experience may be considered


Core Competencies

  • Advanced expertise in Data Management systems and clinical databases

  • Strong project management and organizational skills

  • Proven leadership and people management capabilities

  • Effective problem-solving and decision-making skills

  • Strong stakeholder communication and client engagement experience

  • Ability to manage multiple projects within budget and timelines


About the Organization

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences industry. The organization accelerates drug development and commercialization through advanced analytics, technology, and clinical expertise, supporting improved patient outcomes worldwide.


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