IQVIA, one of the world’s leading healthcare intelligence and clinical research organizations, is hiring Clinical Data Specialist (UAT) professionals across India. This opportunity is ideal for candidates with 2โ5 years of experience in Clinical Data Management (CDM) and User Acceptance Testing (UAT) within clinical trials.
If you have hands-on experience validating edit checks, managing clinical trial databases, and supporting Clinical Data Management activities, this IQVIA recruitment drive could be the next step in your clinical research career.
Job Details
| Particular | Details |
|---|---|
| Company | IQVIA |
| Job Role | Clinical Data Specialist (UAT) |
| Job Type | Full-Time |
| Experience | 2โ5 Years |
| Qualification | Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, Nursing, Biomedical Sciences, or related discipline |
| Location | PAN India |
| Industry | Clinical Research / Clinical Data Management |
| Department | Clinical Data Management (CDM) |
Key Responsibilities
As a Clinical Data Specialist (UAT) at IQVIA, you will be responsible for supporting User Acceptance Testing activities and ensuring clinical trial data quality.
Responsibilities include:
- Perform User Acceptance Testing (UAT) for clinical data management edit checks.
- Create and document test cases within the Data Management Plan.
- Execute testing for edit checks that are ready for UAT.
- Update edit check status in the Data Management Plan and Clinical Trial Database (CTDB).
- Identify, document, and communicate issues related to edit checks.
- Collaborate with programmers to resolve UAT findings.
- Ensure compliance with Standard Operating Procedures (SOPs) and work instructions.
- Support Clinical Data Management processes throughout the clinical trial lifecycle.
- Maintain accurate documentation of testing activities.
- Contribute to high-quality clinical trial data delivery.
Required Qualifications
Candidates should have:
- Bachelor’s or Master’s degree in:
- B.Pharm
- M.Pharm
- Pharm.D
- Life Sciences
- Biotechnology
- Biomedical Sciences
- Nursing
- Or related healthcare discipline
- 2โ5 years of Clinical Data Management experience.
- Hands-on experience in User Acceptance Testing (UAT).
- Strong understanding of Clinical Data Management (CDM) processes.
- Experience with Edit Check validation.
- Knowledge of Clinical Trial Databases (CTDB).
- Good analytical and communication skills.
- Ability to work with cross-functional clinical teams.
Preferred Skills
- Clinical Data Management
- User Acceptance Testing (UAT)
- Clinical Trial Database (CTDB)
- Edit Check Validation
- Data Management Plan
- Clinical Trial Operations
- SOP Compliance
- Defect Tracking
- Clinical Research
- Problem Solving
Why Join IQVIA?
IQVIA offers employees the opportunity to work on global clinical research programs while contributing to healthcare innovation.
Benefits include:
- Global career opportunities
- Exposure to international clinical trials
- Professional development programs
- Learning and certification opportunities
- Inclusive work environment
- Competitive compensation
- Comprehensive employee benefits
- Work with leading pharmaceutical and biotechnology companies
How to Apply
Interested candidates can send their updated resume directly to:
Email: bharathi.n@iqvia.com
Applicants should mention Clinical Data Specialist (UAT) in the email subject line for faster processing.
Apply as early as possible since positions may close once suitable candidates are shortlisted.