IQVIA Hiring Clinical Data Management Specialists
- IQVIA Hiring Clinical Data Management Specialists – High-Paying Pharma Jobs Across India
- Company Overview
- Job Role & Responsibilities
- Clinical Data Management Activities
- EDC System Management
- Data Review & Validation
- Cross-Functional Collaboration
- Eligibility / Qualifications
- Educational Background
- Experience
- Skills Required
- Location & Salary
- Application Process
- Career Growth Opportunities
- Frequently Asked Questions (FAQs)
- What experience is required for this role?
- Which tools are mandatory?
- Is this a remote job?
- What locations are available?
- What is the career scope?
- Job Summary Table
IQVIA Hiring Clinical Data Management Specialists – High-Paying Pharma Jobs Across India
IQVIA is actively hiring Clinical Data Management (CDM) Specialists across multiple locations in India including Kochi, Kolkata, Thane, Bangalore, Pune, and Hyderabad. This opportunity is ideal for experienced professionals (3–7 years) looking to advance their careers in clinical data management, clinical trials, and pharmaceutical research.
This hiring drive focuses on candidates with strong hands-on experience in leading EDC platforms such as Veeva EDC, Medidata Rave, or Oracle Inform. If you have a solid foundation in clinical data handling, validation, and database management, this role offers excellent exposure to global clinical trials and high-growth opportunities.
Company Overview
IQVIA is a global leader in clinical research services, healthcare analytics, and commercial solutions for the life sciences industry. The company plays a critical role in accelerating drug development and improving healthcare outcomes through advanced data science, technology, and domain expertise.
With operations in over 100 countries, IQVIA supports pharmaceutical, biotechnology, and medical device companies in conducting clinical trials, managing real-world evidence, and ensuring regulatory compliance. The organization is known for its innovation-driven approach and strong presence in clinical data management and biostatistics.
IQVIA offers a collaborative work environment, continuous learning programs, and strong career growth pathways, making it one of the most preferred employers in the clinical research industry.
Job Role & Responsibilities
As a Clinical Data Management Specialist, you will be responsible for managing and ensuring the quality, accuracy, and integrity of clinical trial data.
Clinical Data Management Activities
- Lead and support end-to-end clinical data management processes
- Ensure accurate, timely, and high-quality clinical data delivery
- Maintain compliance with regulatory standards and data integrity requirements
EDC System Management
- Configure and manage studies in Veeva EDC, Medidata Rave, or Oracle Inform
- Handle database setup, CRF design, and study configuration
- Support database lock and clinical trial milestones
Data Review & Validation
- Perform data review, discrepancy management, and query resolution
- Conduct validation checks and ensure clean datasets
- Support data cleaning and quality control processes
Cross-Functional Collaboration
- Work closely with Clinical Operations, Biostatistics, and Medical Writing teams
- Contribute to CRF development and database build activities
- Support global clinical trial execution and reporting
This role offers direct exposure to clinical trial lifecycle management and global data operations.
Eligibility / Qualifications
Educational Background
Life Sciences, Pharmacy, Biotechnology, Microbiology, Biochemistry, Clinical Research, Medical Sciences
Experience
- 3 to 7 years of experience in Clinical Data Management
Skills Required
- Strong knowledge of clinical data management processes
- Hands-on experience with Veeva EDC, Medidata Rave, or Oracle Inform
- Understanding of clinical trial lifecycle and regulatory standards
- Strong analytical and problem-solving skills
- Excellent communication and collaboration abilities
- Attention to detail and data accuracy focus
Location & Salary
- Locations: Kochi, Kolkata, Thane, Bangalore, Pune, Hyderabad
- Work Mode: Hybrid (2–3 days onsite)
- Shift: Flexible working hours
- Salary: Not disclosed (highly competitive salary with performance-based growth)
Application Process
Interested candidates can apply by sending their updated CV to the official email ID below:
Email: vaishnavinandkishor.kamble@iqvia.com
Ensure your resume highlights your EDC platform experience, clinical trial exposure, and data management expertise.
Career Growth Opportunities
Professionals in this role can advance into positions such as:
- Senior Clinical Data Manager
- Clinical Data Lead
- Clinical Project Manager
- Biostatistics Analyst
- Clinical Operations Manager
IQVIA provides strong career development programs, global exposure, and opportunities to work on large-scale international clinical trials.
Frequently Asked Questions (FAQs)
What experience is required for this role?
Candidates must have 3–7 years of experience in clinical data management.
Which tools are mandatory?
Hands-on experience with Veeva EDC, Medidata Rave, or Oracle Inform is required.
Is this a remote job?
No, this is a hybrid role with 2–3 days onsite work.
What locations are available?
Kochi, Kolkata, Thane, Bangalore, Pune, and Hyderabad.
What is the career scope?
You can grow into leadership roles in clinical data management, project management, and clinical operations.
Job Summary Table
| Category | Details |
|---|---|
| Company | IQVIA |
| Vacancies | Clinical Data Management Specialist |
| Required Education | Life Sciences, Pharmacy, Biotechnology, Microbiology, Biochemistry, Clinical Research, Medical Sciences |
| Experience | 3–7 Years |
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