IQVIA Hiring Global Data Management Professionals - Multiple Locations
Are you seeking high-paying IQVIA Careers India or Global Data Management Jobs? The leading global Contract Research Organization (CRO) IQVIA has announced massive recruitment for experienced Global Data Management professionals across multiple locations in India. This is a full-time opportunity based in Bangalore, Pune, Hyderabad, Thane, and Kolkata.
Selected candidates will lead clinical data management activities, build and validate databases, design eCRFs, prepare Data Management Plans (DMP), and manage global deliverables. To prepare your profile and get an edge, read our step-by-step guide on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particulars | Details |
|---|---|
| Position | Global Data Management |
| Company | IQVIA |
| Locations | Bangalore, Pune, Hyderabad, Thane, Kolkata (India) |
| Employment Type | Full-Time |
| Experience Required | Experienced Clinical Data Management Professionals |
| Qualifications | B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, Biotech, Life Sciences, Mathematical Sciences |
| Department | Clinical Data Management (CDM) |
| Job ID | R1554421 |
| Salary Package | Competitive (As per experience & industry standards) |
| Application Deadline | July 1, 2026 |
💼 Key Responsibilities
- Lead clinical data management activities across global clinical trials in compliance with study guidelines.
- Design and review Case Report Forms (CRFs) and Electronic Case Report Forms (eCRFs).
- Support database design, build activities, edit check validation, and database setup processes.
- Prepare and update Data Management Plans (DMP) and relevant clinical document guidelines.
- Ensure high-quality deliverables, meet database timelines, and manage clinical database deliverables.
- Provide technical guidance to global project teams, clients, and relevant clinical stakeholders.
- Mentor, train, and develop junior Data Management professionals.
- Conduct regular performance evaluations and project review meetings.
- Manage resource planning, project allocation, and timeline estimations.
- Support proposal development, RFI/RFP requests, and bid defense meetings.
- Participate in study Kick-Off Meetings (KOMs) and client presentation discussions.
- Provide support for regulatory inspections and internal/external quality audits.
- Ensure complete compliance with standard operating procedures (SOPs) and quality standards.
Clinical data management relies heavily on data standards and statistical coordination. If you are comparing career tracks in data management, read our detailed analysis on Clinical SAS vs Clinical Data Management.
🎓 Qualifications & Experience Requirements
Candidates applying for this Global Data Management position should meet the following requirements:
- Education: Bachelor's or Master's Degree in Clinical Sciences, Pharmacy, Biological Sciences, Life Sciences, Biotechnology, Mathematical Sciences, or related fields.
- Eligible Degrees: B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, Lifesciences, Biotechnology, Biological Sciences, Mathematical Sciences.
- Experience: Experienced professional with strong Clinical Data Management expertise.
For pharmacy graduates planning their career paths between domestic clinical roles and overseas careers, check out our guide on B.Pharm Careers: India vs USA.
Required Core Skills
- Hands-on expertise with Medidata Rave EDC or other major EDC systems.
- Experience working on Oncology therapeutic area studies is highly preferred.
- Proven experience in clinical database design, validation, and eCRF builds.
- Familiarity with Good Clinical Practice (GCP) guidelines.
- Strong leadership, people management, and mentoring skills.
- Excellent written and verbal communication and stakeholder management skills.
- Ability to manage project timelines and resource planning.
💰 Salary & Employee Benefits
- Competitive annual compensation package matching experience and industry standards.
- International career growth opportunities in a leading healthcare intelligence company.
- Exposure to state-of-the-art clinical technologies and advanced data tools.
- Collaborative and diverse global working teams.
- Therapeutic area training, specifically in complex Oncology clinical trials.
- Stable career progression and continuous learning programs.
To understand typical roles and career progressions in clinical research coordination and operations, read our comprehensive Clinical Research Coordinator (CRC) Guide.
🌟 Why Join IQVIA?
- IQVIA is one of the world's largest CRO organizations, offering massive scale and global exposure.
- Works with advanced clinical technologies, allowing professionals to build expertise in modern data management platforms.
- Focuses on employee development and provides clear paths to leadership positions.
📑 Resume Tips for Data Management Roles
- Highlight your database design, build, and validation experience using Medidata Rave EDC.
- Clearly describe your experience in therapeutic areas, especially Oncology studies.
- Mention instances where you led team deliverables, trained junior members, or participated in bid defenses.
🎯 IQVIA Global Data Management Interview Questions
- What are the key steps involved in the database design and validation process?
- Explain the purpose of a Data Management Plan (DMP) and what it typically contains.
- How do you handle discrepancy database queries during a clinical trial database lock?
- What is Medidata Rave EDC and how do you configure custom edit check validation rules?
- Describe your experience in Oncology studies and what makes Oncology clinical data management challenging.
📌 How to Apply?
Interested and eligible candidates can submit their applications online directly through IQVIA's official Workday job portal using the link below. The application deadline is **July 1, 2026**. For step-by-step guidance on setting up your application profile, read our guide on how to apply for healthcare and pharma jobs online.
🚀 Apply Now
Apply Online❓ Frequently Asked Questions
Q. What is the application deadline?
The application window is scheduled to close on July 1, 2026.
Q. Who is eligible to apply?
Candidates holding B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, Life Sciences, Biotech, Biological or Mathematical Sciences with Clinical Data Management experience.
Q. What locations are available for this role?
The role is open across IQVIA offices in Bangalore, Pune, Hyderabad, Thane, and Kolkata.
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