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Clinical Research Job in Bengaluru at IQVIA

Looking for a high-growth Clinical Research Job in the pharmaceutical and healthcare industry? The latest opening from IQVIA Jobs for Clinical Data Management professionals offers an incredible opportunity to work on global clinical trials while building a rewarding Clinical Data Management Career. This role is ideal for experienced life science professionals seeking flexible work opportunities, advanced technology exposure, and a strong opportunity for life science graduates in the clinical research sector.

About IQVIA

IQVIA is a globally recognized healthcare and clinical research organization specializing in advanced analytics, technology solutions, and contract research services for the pharmaceutical and healthcare sectors. The company supports clinical development, real-world evidence generation, and healthcare innovation worldwide. Through its advanced clinical research ecosystem, IQVIA offers outstanding Clinical Data Management Career opportunities and serves as a leading destination for professionals seeking a long-term Clinical Research Job in life sciences.

Job Details:

  • Job Title: Clinical Data Management Specialist
  • Location: Bengaluru
  • Job Type: Full-Time | Home-Based

Job Overview

The Clinical Data Management Specialist is responsible for managing end-to-end delivery of data management services for single or multi-service clinical projects with minimal supervision. The role focuses on ensuring high-quality deliverables within agreed timelines and budgets while maintaining customer satisfaction.

The position involves leadership responsibilities within the Data Management (DM) team, including project planning, execution, financial oversight, communication management, and milestone tracking. The selected candidate will also perform the role of Data Team Lead (DTL).

Key Responsibilities

  • Study Setup & Data Management
    • Gather study setup requirements through collaboration with relevant stakeholders.
    • Support and oversee validation of new device integrations with minimal guidance.
    • Perform and monitor routine data cleaning activities to ensure high-quality and timely data delivery.
    • Ensure all deliverables meet expected quality standards and sponsor expectations.
    • Assist in ensuring services and deliverables align with agreed timelines and Scope of Work (SOW).
  • Project Coordination & Leadership
    • Lead internal study meetings and support sponsor meetings, audits, and study kick-off sessions.
    • Track project progress, identify risks, and implement corrective actions when required.
    • Oversee implementation of new technologies and database revisions with guidance.
    • Support training and onboarding of new team members.
    • Collaborate with programming teams for process innovation and automation initiatives.
  • Compliance & Process Improvement
    • Maintain compliance with trainings and eSOP requirements.
    • Review and contribute to development, revision, and maintenance of operational procedures and work instructions.
    • Ensure collaborative communication with line managers and cross-functional teams.
    • Perform additional responsibilities as assigned by the Line Manager.

Required Qualifications

  • Educational Qualification
    • Bachelor’s Degree in:
      • Clinical Sciences
      • Biological Sciences
      • Related disciplines
  • Experience Requirements
    • 3–4 years of direct Clinical Data Management experience
    • Minimum 1 year of hands-on experience with Veeva EDC
    • Strong understanding of:
      • Drug development lifecycle
      • Clinical research processes
      • Data management workflows
  • Technical Skills
    • Advanced proficiency in:
      • Microsoft Excel
      • Microsoft Word
      • Email and collaboration tools
    • Experience with:
      • Data cleaning and validation
      • Clinical databases
      • Process automation and innovation initiatives
  • Language Requirements
    • Advanced spoken and written English proficiency
  • Preferred Competencies
    • Leadership and project coordination abilities
    • Strong analytical and problem-solving skills
    • Ability to manage timelines and stakeholder expectations
    • Collaborative mindset for cross-functional teamwork
    • Attention to detail and quality compliance

APPLY ONLINE HERE

Diluxi Arya
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