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Global Data Management

IQVIA
2-4 years
INR 15 LPA – 24 LPA
Hyderabad
1 June 29, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance

Global Data Management

Company: IQVIA
Location: Hyderabad, India
Department: Global Clinical Data Management (CDM)
Job Type: Full-Time
Work Mode: Hybrid

JOB OVERVIEW

The Global Data Management professional is responsible for leading Clinical Data Management (CDM) activities across global clinical trials by ensuring the timely delivery of high-quality, compliant, and accurate clinical data. The role involves CRF/eCRF design, database setup, data validation, study planning, project oversight, team leadership, staff mentoring, proposal support, operational excellence, and collaboration with internal and external stakeholders to ensure successful execution of clinical research programs.

KEY RESPONSIBILITIES

Clinical Data Management

  • Lead Clinical Data Management activities for global clinical studies.

  • Review and approve Data Management deliverables.

  • Oversee CRF and eCRF design and development.

  • Manage clinical database design and setup.

  • Ensure timely delivery of high-quality clinical databases.

Database Development & Validation

  • Define database validation specifications.

  • Support database programming and testing.

  • Review edit checks and validation rules.

  • Ensure database quality and data integrity.

  • Maintain compliant database deliverables.

Project Leadership

  • Support study start-up and project planning activities.

  • Monitor project timelines, budgets, and deliverables.

  • Identify project risks and implement mitigation strategies.

  • Coordinate staffing and workload planning.

  • Ensure successful execution of global projects.

Team Management & Mentorship

  • Mentor Clinical Data Management professionals.

  • Conduct regular performance and development discussions.

  • Identify training and professional development needs.

  • Monitor team utilization and productivity.

  • Promote employee engagement and continuous learning.

Operational Excellence

  • Provide technical guidance to internal and external stakeholders.

  • Support proposal development, RFIs, RFPs, and budgeting.

  • Participate in bid defenses and project kick-off meetings.

  • Improve Clinical Data Management processes and operational efficiency.

  • Support strategic planning and resource management.

Compliance & Quality Assurance

  • Ensure compliance with SOPs, ICH-GCP, and regulatory guidelines.

  • Maintain inspection-ready documentation.

  • Support internal and external audits and inspections.

  • Monitor compliance with project scope and quality standards.

  • Drive continuous quality improvement initiatives.

Stakeholder Collaboration

  • Collaborate with Clinical Operations, Programming, Biostatistics, Project Management, and Sponsors.

  • Communicate project status, risks, and operational updates.

  • Provide technical solutions to improve study efficiency.

  • Build strong relationships with global teams and clients.

  • Ensure consistent execution across multiple clinical programs.

EDUCATIONAL QUALIFICATIONS

Required

Bachelor's Degree in:

  • Clinical Sciences

  • Biological Sciences

  • Life Sciences

  • Pharmacy

  • Biotechnology

  • Mathematics

  • Statistics

  • Or a related discipline

Equivalent education and relevant experience may also be considered.

EXPERIENCE REQUIREMENTS

Required

Experience in:

  • Clinical Data Management (CDM)

  • Global Clinical Trials

  • Oncology Clinical Studies

  • Medidata Rave EDC

  • Clinical Database Design

  • Database Setup and Validation

Preferred

  • Experience leading Clinical Data Management teams.

  • Proposal development and bid defense participation.

  • Budget planning and resource management.

  • Audit and inspection support.

  • Knowledge of CDISC standards and Electronic Data Capture (EDC) systems.