Apply for IQVIA IRT Coordinator pharma jobs for freshers and experienced candidates. Check eligibility, salary details, and apply online today.
Introduction
The pharmaceutical and clinical research industry continues to expand rapidly, creating new opportunities for skilled professionals in clinical technology roles. One such exciting opportunity is the IRT Coordinator role at IQVIA, a globally recognized leader in healthcare intelligence and clinical research services. This position offers hands-on exposure to clinical trial systems, cross-functional collaboration, and global project execution. If you are looking to build a career in clinical data systems and trial management, this role can be a strong stepping stone.
Job Overview
| Details | Information |
|---|---|
| Job Title | IRT Coordinator |
| Company Name | IQVIA |
| Location | Bengaluru, Karnataka, India |
| Employment Type | Full-Time (Remote Option Available) |
| Department | Clinical Trials / IRT Management |
| Experience Required | 1–3 Years |
| Education | Diploma / Degree in Life Sciences or related field |
| Salary | As per company norms |
Company Overview
IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. The company supports pharmaceutical, biotechnology, and healthcare organizations in accelerating drug development and improving patient outcomes. With operations across multiple countries, IQVIA is known for innovation, data-driven solutions, and strong clinical expertise.
Job Location & Employment Type
This role is based in Bengaluru, India, with a remote working option, making it flexible for professionals seeking hybrid work opportunities. It is a full-time permanent position within the clinical trial technology domain.
Open Positions / Department Details
The position falls under the Interactive Response Technology (IRT) / Clinical Data Management (CDM) function. The IRT team plays a crucial role in managing clinical trial systems that handle subject randomization, drug supply logistics, and trial data tracking.
Key Roles & Responsibilities
As an IRT Coordinator, you will contribute to the smooth execution of clinical trials by supporting system operations and coordination tasks. Your responsibilities include:
- Assisting in preparation of IRT-related documentation for study start-up and ongoing phases
- Creating user guides, test scripts, and system documentation using standard templates
- Supporting database testing and validating system functionality
- Participating in User Acceptance Testing (UAT) with cross-functional teams
- Managing drug inventory tracking and assisting with supply orders
- Generating reports and verifying accuracy of outputs
- Supporting data transfer activities as per study requirements
- Maintaining documentation within electronic Trial Master File (eTMF)
- Coordinating internal and client meetings
- Providing technical and user support for IRT systems
- Troubleshooting issues and escalating when required
- Contributing to process improvements and knowledge-sharing initiatives
Eligibility Criteria
Education
- Diploma, Bachelor’s, or equivalent qualification in Life Sciences, Pharmacy, Biotechnology, or related field
Experience
- 1 to 3 years of relevant experience in clinical trials, data management, or IRT systems
Skills Required
- Basic understanding of clinical trial processes and protocols
- Knowledge of IRT systems, randomization, and drug supply management
- Familiarity with GxP and ICH-GCP guidelines
- Experience with documentation such as URS, UAT scripts, and validation records
- Strong coordination and project management skills
- Good communication skills for global team collaboration
- Ability to handle data entry, reporting, and system updates
Salary & Benefits
- Salary: As per company norms
- Opportunity to work with global clinical teams
- Exposure to advanced clinical technologies and systems
- Career growth in clinical research and data management
- Flexible work environment (remote/hybrid options)
Selection Process
The hiring process typically includes:
- Application Screening
- HR Interview
- Technical / Functional Interview
- Final Discussion with Hiring Manager
How to Apply
Interested candidates can apply through the online application method via the official company career portal or job listing platform.
Important Dates
- Application Status: Open (Apply as soon as possible)
Why Apply for This Job?
The IRT Coordinator job at IQVIA offers a strong foundation in clinical trial technology and operations. Here’s why this role stands out:
- Work with one of the top global clinical research organizations
- Gain practical experience in IRT systems and clinical trial workflows
- Enhance your profile in data management and clinical operations
- Build international exposure through cross-functional collaboration
- Opportunity to grow into advanced roles like IRT Specialist or Clinical Data Manager
This role is especially valuable for candidates aiming to transition into clinical research technology or data-driven roles in pharma.
FAQs
1. What is the role of an IRT Coordinator?
An IRT Coordinator supports clinical trials by managing systems used for patient randomization, drug supply tracking, and trial data handling.
2. Who can apply for this job?
Candidates with a life sciences or pharmacy background and 1–3 years of experience in clinical research or data management can apply.
3. Is this job suitable for freshers?
This role requires some prior experience, but candidates with internships or relevant exposure may also be considered.
4. What is the salary for an IRT Coordinator at IQVIA?
The salary is not disclosed but is offered as per company standards and industry benchmarks.
5. How can I apply for this job?
You can apply online through IQVIA’s official careers page or job portals where the listing is published.
Conclusion
The IRT Coordinator opportunity at IQVIA is an excellent career option for professionals interested in clinical trial systems and data management. With global exposure, structured learning, and career advancement opportunities, this role can significantly strengthen your position in the pharmaceutical and clinical research industry. Apply early to secure your chance.
Disclaimer
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